Author:
Morton Sarah U.,Joshi Mugdha,Savic Talia,Beggs Alan H.,Agrawal Pankaj B.
Publisher
Public Library of Science (PLoS)
Reference35 articles.
1. Approach to the diagnosis of congenital myopathies;KN North;Neuromuscul Disord,2014
2. Congenital myopathies—a comprehensive update of recent advancements;MC Sharma;Acta Neurol Scand,2009
3. Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2;PB Agrawal;Am J Hum Genet,2007
4. Congenital myopathy caused by a novel missense mutation in the CFL2 gene;CW Ockeloen;Neuromuscul Disord,2012
5. Ong RW, Alsaman A, Selcen D, Arabshahi A, Yau KS, Ravenscroft G, et al. (2014) Novel cofilin-2 (CFL2) four base pair deletion causing nemaline myopathy. J Neurol Neurosurg Psychiatry.
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献