Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Satyanarayana Matsa Lova"'
Publikováno v:
Gene Reports. 8:94-99
Hypertrophic cardiomyopathy is a multifactorial disorder, with mutations implicated in 12 sarcomeric and cytoskeletal genes accounting for genotypic and phenotypic heterogeneity, making genetic and clinical diagnosis much more challenging. The geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4264e101fdc4850304f2bb39c9f1117e
https://doi.org/10.1016/j.genrep.2017.06.004
https://doi.org/10.1016/j.genrep.2017.06.004
Publikováno v:
Current Research: Cardiology. 2
background: Hypertrophic cardiomyopathy (HCM) is a multifactorial disorder, with mutations implicated in 14 sarcomeric and cytoskeletal genes, leading to genotypic and phenotypic heterogeneity, and a challenging genetic and clinical diagnosis. The ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba85b1b315c9783edfd67f97ea622fbe
https://doi.org/10.4172/2368-0512.1000021
https://doi.org/10.4172/2368-0512.1000021
Publikováno v:
International Journal of Genetics and Genomics. 2:84
Hypertrophic cardiomyopathy is an autosomal dominant disorder, characterized by thickening of the myocardium with a variable clinical course. Mutations in 14 sarcomeric genes have been implicated resulting in phenotypic and genotypic heterogeneity. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04fb5a02dc16e67891fbbaf283388dd6
https://doi.org/10.11648/j.ijgg.20140205.12
https://doi.org/10.11648/j.ijgg.20140205.12
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