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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| 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. |
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| 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 |
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