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MRI findings in X-linked Charcot–Marie–Tooth disease associated with a novel connexin 32 mutation

✍ Scribed by J.M. U-King-Im; E. Yiu; E.J. Donner; M. Shroff


Book ID
116389077
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
714 KB
Volume
66
Category
Article
ISSN
0009-9260

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by R d G. Worton Charcot-Marie tooth disease, a pathologically and genetically heterogeneous group of disorders that causes a progressive neuropathy, is characterized by weakness and atrophy, primarily in peroneal and distal leg muscles. It is defined patholog-Mutation leads to 10s:. of this Mae 111