Congenital myasthenic syndromes due to mutations inALG2andALG14-Reference-Cited by-同舟云学术

Congenital myasthenic syndromes due to mutations inALG2andALG14

Published:2013-02-11 Issue:3 Volume:136 Page:944-956
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Cossins Judith,Belaya Katsiaryna,Hicks Debbie,Salih Mustafa A.,Finlayson Sarah,Carboni Nicola,Liu Wei Wei,Maxwell Susan,Zoltowska Katarzyna,Farsani Golara Torabi,Laval Steven,Seidhamed Mohammed Zain,Donnelly Peter,Bentley David,McGowan Simon J.,Müller Juliane,Palace Jacqueline,Lochmüller Hanns,Beeson David,

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/136/3/944/13796469/awt010.pdf

Reference35 articles.

1. TEXtopo: shaded membrane protein topology plots in LATEX2

2. Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates

3. Structure, Expression, and Regulation of UDP-GlcNAc: Dolichol Phosphate GlcNAc-1-Phosphate Transferase (DPAGT1)

4. 186th ENMC International Workshop: Congenital myasthenic syndromes 24–26 June 2011, Naarden, The Netherlands

5. Current status of the congenital myasthenic syndromes

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