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

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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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Bibliographic Details
Main Author:	Sarimah , Samulong
Format:	Thesis
Published:	2016
Subjects:	R Medicine (General)
Online Access:	http://studentsrepo.um.edu.my/7040/ http://studentsrepo.um.edu.my/7040/4/sarimah.pdf

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