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News: ESHG 2017 Copenhagen Talk - Exome sequencing in Cardiomyopathy Apr 11, 2017; New Project Funding to investigate congenital forms of muscular dystrophy Apr 11, 2017; Genetic study identifies a new form of congenital muscular dystrophy Feb 20, 2017; New intern in the lab Sep 19, 2016; Paper: Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease Feb 25, 2016