Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families

BACKGROUND: The genetic basis for dilated cardiomyopathy (DCM) can be difficult to determine, particularly in familial cases with complex phenotypes. Next generation sequencing may be useful in the management of such cases. METHODS: We report two large families with pleiotropic inherited cardiomyopa...

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發表在:BMC Med Genet
Main Authors: Hanley, Alan, Walsh, Katie A., Joyce, Caroline, McLellan, Michael A., Clauss, Sebastian, Hagen, Amaya, Shea, Marisa A., Tucker, Nathan R., Lin, Honghuang, Fahy, Gerard J., Ellinor, Patrick T.
格式: Artigo
語言:Inglês
出版: BioMed Central 2016
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5114776/
https://ncbi.nlm.nih.gov/pubmed/27855642
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0347-6
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