MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypes-Reference-Cited by-同舟云学术

MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypes

Published:2018-01 Issue:1 Volume:28 Page:48-53
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Harris Elizabeth,Marini-Bettolo Chiara,Töpf Ana,Barresi Rita,Polvikoski Tuomo,Bailey Geraldine,Charlton Richard,Tellez James,MacArthur Daniel,Guglieri Michela,Lochmüller Hanns,Bushby Kate,Straub Volker

Funder

Medical Research Council UK

European Union Seventh Framework Programme

Muscular Dystrophy UK Clinical Training and Research Fellowship

US National Institutes of Health

Publisher

Elsevier BV

Subject

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

Reference15 articles.

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4. Megf10 is a receptor for C1Q that mediates clearance of apoptotic cells by astrocytes;Iram;J Neurosci,2016

5. Jedi-1 and MEGF10 signal engulfment of apoptotic neurons through the tyrosine kinase Syk;Scheib;J Neurosci,2012

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