Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

10.1371/journal.pone.0172995

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Bibliographic Details
Main Authors:	Esslinger U., Garnier S., Korniat A., Proust C., Kararigas G., Müller-Nurasyid M., Empana J.-P., Morley M.P., Perret C., Stark K., Bick A.G., Prasad S.K., Kriebel J., Li J., Tiret L., Strauch K., O'Regan D.P., Marguiles K.B., Seidman J.G., Boutouyrie P., Lacolley P., Jouven X., Hengstenberg C., Komajda M., Hakonarson H., Isnard R., Arbustini E., Grallert H., Cook S.A., Seidman C.E., Regitz-Zagrosek V., Cappola T.P., Charron P., Cambien F., Villard E.
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2019
Subjects:	ALPK3 gene Article BAG3 gene computer model congestive cardiomyopathy controlled study exome female FHOD3 gene FLNC gene gene gene expression gene function gene identification gene locus gene mapping gene mutation genetic susceptibility genome-wide association study genotype HSPB7 gene human human cell human tissue major clinical study male missense mutation MLIP gene population research single nucleotide polymorphism SLC39A8 gene TTN gene ZBTB17 gene genetic predisposition genetics Cardiomyopathy, Dilated Exome Genetic Predisposition to Disease Humans Mutation, Missense Polymorphism, Single Nucleotide
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/161526
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Institution:	National University of Singapore

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