Identification of mutations in genes commonly associated with charcot-marie-tooth disease in a malaysian cohort and a survey on the malaysian perspective of rare disorders / Sarimah Samulong
Charcot-Marie-Tooth (CMT) disease is the most common form of an inherited neuromuscular disorder with an incidence of 1 in 2500. CMT can be classified into demyelinating (CMT1) or axonal (CMT2) subtypes. CMT is typically diagnosed based on clinical and electrophysiological studies, together with gen...
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| Format: | Thesis |
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2016
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| Online Access: | http://studentsrepo.um.edu.my/7040/4/sarimah.pdf http://studentsrepo.um.edu.my/7040/ |
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