Mutations in theMORC2gene cause axonal Charcot–Marie–Tooth disease-Reference-Cited by-同舟云学术

Mutations in theMORC2gene cause axonal Charcot–Marie–Tooth disease

Published:2015-10-24 Issue:1 Volume:139 Page:62-72
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Sevilla Teresa,Lupo Vincenzo,Martínez-Rubio Dolores,Sancho Paula,Sivera Rafael,Chumillas María J.,García-Romero Mar,Pascual-Pascual Samuel I.,Muelas Nuria,Dopazo Joaquín,Vílchez Juan J.,Palau Francesc,Espinós Carmen

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/139/1/62/17348056/awv311.pdf

Reference31 articles.

1. Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V

2. Recent advances in Charcot–Marie–Tooth disease

3. A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation

4. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations

5. Different clinical and magnetic resonance imaging features between Charcot–Marie–Tooth disease type 1A and 2A

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