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X-linked dominant charcot–marie–tooth neuropathy with 15 cases in a family genetic linkage study

✍ Scribed by Dr. Victor V. Ionasescu; Dr. Trudy L. Burns; Mr. Charles Searby; Dr. Rebecca Ionasescu


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
234 KB
Volume
11
Category
Article
ISSN
0148-639X

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In a cross-sectional, clinical, and morphometric analysis we assessed the correlation between the clinical and pathological evolution of disease in 20 unrelated patients of various ages affected by Charcot-Marie-Tooth neuropathy type 1A (CMT1A) with the 17p11.2p12 (peripheral myelin protein 22, PMP2