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. - Ben Yaou, R.; Gerard, M.; Chami, K.; Sehier, A.; Belin, A.; Labombarda, F.; Richard, P.; Bonne, G.; Leturcq, F.; Chapon, F. (Neuromuscular Disorders, 2014)