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BIOPHYSICAL CHARACTERIZATION OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY-RELATED TROPONIN T MUTATIONS

✍ Scribed by Li, A.Y.; Liang, B.; Tibbits, G.


Book ID
127174546
Publisher
Pulsus Group Inc
Year
2014
Tongue
English
Weight
136 KB
Volume
30
Category
Article
ISSN
0828-282X

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Mutations in the human cardiac troponin T gene (TNNT2) are associated with familial hypertrophic cardiomyopathy (FHC) linked to chromosome 1q3 (CMH2). Mutation analyses of TNNT2 have been restricted to RNA-based screening methods because only the TNNT2 cDNA sequence was known. We characterized the g