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Abbreviation : CMT1E
Long Form : CMT type 1 E
No. Year Title Co-occurring Abbreviation
2022 Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients. CMT1A, HNPP, PMP22, TS, WES
2013 Parental mosaicism of a novel PMP22 mutation with a minimal neuropathic phenotype. CMT, PMP22, SNAPs