A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene-Reference-Cited by-同舟云学术

A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene

Published:2000-07 Issue:1 Volume:67 Page:37-46
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Mersiyanova Irina V.,Perepelov Alexander V.,Polyakov Alexander V.,Sitnikov Vladimir F.,Dadali Elena L.,Oparin Roman B.,Petrin Alexander N.,Evgrafov Oleg V.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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3. Localisation of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity;Ben Othmane;Genomics,1993

4. Connexin mutation in X-linked Charcot-Marie-Tooth disease;Bergoffen;Science,1993

5. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study;Birouk;Neurology,1998

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