Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)-Reference-Cited by-同舟云学术

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

Published:2011-11-20 Issue:12 Volume:43 Page:1189-1192
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Logan Clare V,Lucke Barbara,Pottinger Caroline,Abdelhamed Zakia A,Parry David A,Szymanska Katarzyna,Diggle Christine P,van Riesen Anne,Morgan Joanne E,Markham Grace,Ellis Ian,Manzur Adnan Y,Markham Alexander F,Shires Mike,Helliwell Tim,Scoto Mariacristina,Hübner Christoph,Bonthron David T,Taylor Graham R,Sheridan Eamonn,Muntoni Francesco,Carr Ian M,Schuelke Markus,Johnson Colin A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.995.pdf

Reference15 articles.

1. Grohmann, K. et al. Nat. Genet. 29, 75–77 (2001).

2. Guenther, U.P. et al. J. Mol. Med. 87, 31–41 (2009).

3. Guenther, U.P. et al. Hum. Mutat. 28, 808–815 (2007).

4. Grohmann, K. et al. Hum. Mol. Genet. 13, 2031–2042 (2004).

5. Maddatu, T.P. et al. Hum. Mol. Genet. 13, 1105–1115 (2004).

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