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Mutation analysis in Charcot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity

✍ Scribed by P. Young; K. Grote; G. Kuhlenbäumer; O. Debus; H. Kurlemann; H. Halfter; H. Funke; E. B. Ringelstein; F. Stögbauer

Publisher
Springer
Year
2001
Tongue
English
Weight
258 KB
Volume
248
Category
Article
ISSN
0340-5354

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