An in silico analysis of troponin I mutations in hypertrophic cardiomyopathy of Indian origin. [electronic resource]
- PloS one 2013
- e70704 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0070704 doi
Amino Acid Sequence Amino Acid Substitution Cardiomyopathy, Hypertrophic--genetics Humans India Models, Molecular Molecular Sequence Data Mutation Polymorphism, Single Nucleotide Protein Binding Protein Conformation Sequence Alignment Troponin C--chemistry Troponin I--chemistry White People--genetics