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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