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Abbreviation : CMT1A
Long Form : caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12
No. Year Title Co-occurring Abbreviation
2002 [Molecular genetic diagnosis of Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies]. CMT, HNPP, PCR, PMP22
2001 Molecular genetic analysis of Charcot-Marie-Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging. CMT1, PSL