An In Silico Analysis of Troponin I Mutations in Hypertrophic Cardiomyopathy of Indian Origin

Hypertrophic Cardiomyopathy (HCM) is an autosomal dominant disorder of the myocardium which is hypertrophied resulting in arrhythmias and heart failure leading to sudden cardiac death (SCD). Several sarcomeric proteins and modifier genes have been implicated in this disease. Troponin I, being a part...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ramachandran, Gayatri, Kumar, Manoj, Selvi Rani, Deepa, Annanthapur, Venkateshwari, Calambur, Narasimhan, Nallari, Pratibha, Kaur, Punit
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2013
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3742764/
https://ncbi.nlm.nih.gov/pubmed/23967088
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0070704
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