Two recurrent mutations are associated with GNE myopathy in the North of Britain-Reference-Cited by-同舟云学术

Two recurrent mutations are associated with GNE myopathy in the North of Britain

Published:2014-04-02 Issue:12 Volume:85 Page:1359-1365
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Chaouch Amina,Brennan Kathryn M,Hudson Judith,Longman Cheryl,McConville John,Morrison Patrick J,Farrugia Maria E,Petty Richard,Stewart Willie,Norwood Fiona,Horvath Rita,Chinnery Patrick F,Costigan Donald,Winer John,Polvikoski Tuomo,Healy Estelle,Sarkozy Anna,Evangelista Teresinha,Pogoryelova Oksana,Eagle Michelle,Bushby Kate,Straub Volker,Lochmüller Hanns

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference29 articles.

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5. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy;Eisenberg;Nat Genet,2001

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