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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Slovenian Medical Association
2003-10-01
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Series: | Zdravniški Vestnik |
Subjects: | |
Online Access: | http://vestnik.szd.si/index.php/ZdravVest/article/view/1873 |