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G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features.

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Bibliographic Details
Title:	G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features.
Authors:	Ben Yaou, R.¹, Gerard, M.², Chami, K.³, Sehier, A.², Belin, A.⁴, Labombarda, F.⁴, Richard, P.⁵, Bonne, G.⁶, Leturcq, F.⁷, Chapon, F.⁴
Source:	Neuromuscular Disorders. Oct2014, Vol. 24 Issue 9/10, p843-844. 2p.
Database:	Academic Search Ultimate

Description
ISSN:	09608966
DOI:	10.1016/j.nmd.2014.06.172