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
✦ LIBER ✦
Hypertrophic Cardiomyopathy. A Study of the Troponin-T Gene in 127 Spanish Families
✍ Scribed by Juan R. Gimeno; Lorenzo Monserrat; Inmaculada Pérez-Sánchez; Francisco Marín; Luis Caballero; Manuel Hermida-Prieto; Alfonso Castro; Mariano Valdés
- Book ID
- 119643656
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 149 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1885-5857
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