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<entry xmlns:xsd="http://www.w3.org/2001/XMLSchema" xmlns:env="http://schemas.xmlsoap.org/soap/envelope/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" query="LQT1">
<item seqid="0">
  <pair_id xsi:type="xsd:int">3053927</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long QT syndrome type 1</long_form>
  <pair_number xsi:type="xsd:int">77</pair_number>
</item>
<item seqid="1">
  <pair_id xsi:type="xsd:int">3053919</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS type 1</long_form>
  <pair_number xsi:type="xsd:int">20</pair_number>
</item>
<item seqid="2">
  <pair_id xsi:type="xsd:int">3053928</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long QT1</long_form>
  <pair_number xsi:type="xsd:int">4</pair_number>
</item>
<item seqid="3">
  <pair_id xsi:type="xsd:int">3053908</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long-QT type 1</long_form>
  <pair_number xsi:type="xsd:int">4</pair_number>
</item>
<item seqid="4">
  <pair_id xsi:type="xsd:int">3053922</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">25-lead electrocardiograms in nine asymptomatic KCNQ1 mutation carriers</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="5">
  <pair_id xsi:type="xsd:int">3053899</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">located on chromosome 7 and KVLQT1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="6">
  <pair_id xsi:type="xsd:int">3053900</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">location of mutations across KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="7">
  <pair_id xsi:type="xsd:int">3053901</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long QT syndrome due to KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="8">
  <pair_id xsi:type="xsd:int">3053902</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long QT syndrome genes, namely, KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="9">
  <pair_id xsi:type="xsd:int">3053903</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long QT syndrome genotypes in KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="10">
  <pair_id xsi:type="xsd:int">3053926</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">long-QT1 syndrome</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="11">
  <pair_id xsi:type="xsd:int">3053923</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQT genes have been identified: KVLQT1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="12">
  <pair_id xsi:type="xsd:int">3053924</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQT has been identified on chromosome 11p15.5</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="13">
  <pair_id xsi:type="xsd:int">3053925</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQT loci on chromosomes 11</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="14">
  <pair_id xsi:type="xsd:int">3053920</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQT syndrome type 1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="15">
  <pair_id xsi:type="xsd:int">3053921</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQT1 but not in control patients during epinephrine</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="16">
  <pair_id xsi:type="xsd:int">3053912</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQT3 are caused by mutations in KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="17">
  <pair_id xsi:type="xsd:int">3053913</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS associated with missense variants in KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="18">
  <pair_id xsi:type="xsd:int">3053914</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS caused by the KCNQ1 potassium channel gene mutations</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="19">
  <pair_id xsi:type="xsd:int">3053915</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS due to mutation of the KCNQ1 gene</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="20">
  <pair_id xsi:type="xsd:int">3053916</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS genes; KCNQ1/KVLQT1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="21">
  <pair_id xsi:type="xsd:int">3053917</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS genotypes included type 1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="22">
  <pair_id xsi:type="xsd:int">3053918</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS have been mapped to chromosome 11p15.5</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="23">
  <pair_id xsi:type="xsd:int">3053910</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS-associated genes KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="24">
  <pair_id xsi:type="xsd:int">3053911</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS-causing channel genes, KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="25">
  <pair_id xsi:type="xsd:int">3053904</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS-causing mutations in KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="26">
  <pair_id xsi:type="xsd:int">3053905</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS-causing potassium channel genes: KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="27">
  <pair_id xsi:type="xsd:int">3053906</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS-susceptibility genes: KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
<item seqid="28">
  <pair_id xsi:type="xsd:int">3053907</pair_id>
  <abbreviation xsi:type="xsd:string">LQT1</abbreviation>
  <long_form xsi:type="xsd:string">LQTS: KCNQ1</long_form>
  <pair_number xsi:type="xsd:int">1</pair_number>
</item>
</entry>
