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

• 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.
• 其他作者: DUKE-NUS MEDICAL SCHOOL
• 格式: Article
• 出版: 2019
• 主題: 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
• 在線閱讀: https://scholarbank.nus.edu.sg/handle/10635/161526

10.1371/journal.pone.0172995