Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores-Reference-Cited by-同舟云学术

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

Published:2010-12 Issue:6 Volume:87 Page:842-847
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference25 articles.

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4. 161st ENMC International Workshop on nemaline myopathy and related disorders, Newcastle upon Tyne, 2008;Laing;Neuromuscul Disord.,2009

5. What's new in congenital myopathies?;North;Neuromuscul. Disord.,2008

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