THE MOST FREQUENT TYPES OF DEMYELINATIVE CHARCOT-MARIE-TOOTH DISEASE IN SLOVENIA: A POPULATION-BASED STUDY

<p>Background. The most common genetic defect in demyelinative type of Charcot-Marie-Tooth disease (CMT1) is dominantly inherited duplication of 17p11.2 (CMT1A). Phenotipically rather different, but genetically related to CMT1A, is hereditary neuropathy with liability to pressure palsies (HNPP...

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Bibliographic Details
Main Authors: Lea Leonardis, Janez Zidar, Borut Peterlin
Format: Article
Language:English
Published: Slovenian Medical Association 2003-10-01
Series:Zdravniški Vestnik
Subjects:
Online Access:http://vestnik.szd.si/index.php/ZdravVest/article/view/1873