A rapid protocol for cardiac troponin T
โ
Brenda Gerull; Karl-Josef Osterziel; Christian Witt; Rainer Dietz; Ludwig Thierf
๐
Article
๐
1998
๐
John Wiley and Sons
๐
English
โ 143 KB
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