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Paper: Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease

Paper accepted: "Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease" in the International Journal of Cardiology

Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease
M. Muggenthaler, E. Petropoulou, S. Omer, M.A. Simpson, H. Sahak, A. Rice, H. Raju, F.J. Conti, L.R. Bridges, L.J. Anderson, S. Sharma, E.R. Behr, Y. Jamshidi
Publication stage: In Press Accepted Manuscript
International Journal of Cardiology
Published online: February 13 2016

 

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