Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes-Reference-Cited by-同舟云学术

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Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes

Published:2002-10 Issue:7-8 Volume:12 Page:643-650
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Street V.A.,Meekins G.,Lipe H.P.,Seltzer W.K.,Carter G.T.,Kraft G.H.,Bird T.D.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference34 articles.

1. Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field;Nelis;Neurogenetics,2000

2. Charcot–Marie–Tooth disease type 1: molecular pathogenesis to gene therapy;Kamholz;Brain,2000

3. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies;Nelis;Hum Mutat,1999

4. DNA duplication associated with Charcot–Marie–Tooth disease type 1A;Lupski;Cell,1991

5. Connexin mutations in X-linked Charcot–Marie–Tooth disease;Bergoffen;Science,1993

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