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

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

Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Cardiology - Volume 210, 1 May 2016, Pages 41-44

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,