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Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

โœ Scribed by SC Menon; VV Michels; PA Pellikka; JD Ballew; ML Karst; KJ Herron; SM Nelson; RJ Rodeheffer; TM Olson


Book ID
110888663
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
446 KB
Volume
74
Category
Article
ISSN
0009-9163

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A rapid protocol for cardiac troponin T
โœ Brenda Gerull; Karl-Josef Osterziel; Christian Witt; Rainer Dietz; Ludwig Thierf ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 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