Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease.
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| Description | scientific article published on 13 February 2016 |
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author: Yalda Jamshidi Hariharan Raju Elijah Behr Sanjay Sharma |
| Publication date | February 13, 2016 |
| Language | English |
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