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Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores

✍ Scribed by Nyamkhishig Sambuughin; Kyle S. Yau; Montse Olivé; Rachael M. Duff; Munkhuu Bayarsaikhan; Shajia Lu; Laura Gonzalez-Mera; Padma Sivadorai; Kristen J. Nowak; Gianina Ravenscroft; Frank L. Mastaglia; Kathryn N. North; Biljana Ilkovski; Hannie Kremer; Martin Lammens; Baziel G.M. van Engelen; Vicki Fabian; Phillipa Lamont; Mark R. Davis; Nigel G. Laing; Lev G. Goldfarb

Book ID: 113422977
Publisher: American Society of Human Genetics
Year: 2011
Tongue: English
Weight: 38 KB
Volume: 88
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2010.12.013

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