X-Linked Charcot-Marie-Tooth Disease in 93 Patients
DOI:
https://doi.org/10.15844/pedneurbriefs-15-10-5Keywords:
Electrophysiological and Genetic Features, Molecular Genetic Testing, Nonfunctional MutationsAbstract
The clinical, electrophysiological and genetic features of 93 patients (41 males, 52 females) from 37 unrelated families with X-linked dominant Charcot-Marie-Tooth (CMTX) disease are reported from the Hopital de la Salpetriere, Paris, France.Published
2001-10-01
Issue
Section
Degenerative Diseases
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Copyright (c) 2001 The Author(s)
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