Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease
| Autor: | Muggenthaler, M., Petropoulou, E., Omer, S., Simpson, M.A., Sahak, H., Rice, A., Raju, H., Conti, F.J., Bridges, L.R., Anderson, L.J., Sharma, S., Behr, E.R., Jamshidi, Y. |
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| Zdroj: | In International Journal of Cardiology 1 May 2016 210:41-44 |
| Databáze: | ScienceDirect |
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