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, MA, Sahak, H, Rice, A, Raju, H, Conti, FJ, Bridges, LR, Anderson, LJ, Sharma, S, Behr, ER, Jamshidi, Y |
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| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Zdroj: | International Journal of Cardiology |
| Databáze: | OpenAIRE |
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