Genetic heterogeneity of hypertrophic cardiomyopathy
โ Scribed by Branzi, A.; Romeo, G.; Specchia, S.; Lolli, C.; Binetti, G.; Devoto, M.; Bacchi, M.; Magnani, B.
- Book ID
- 122908770
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 312 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0167-5273
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
To understand the molecular basis of familial hypertrophic cardiomyopathy (FHC) in the Chinese population, a family with FHC was investigated. Nineteen family members who were 16 years of age or older were examined by M-mode or two-dimensional echocardiography. Eight members were diagnosed to be aff
## Abstract ## BACKGROUND Nonsyndromic hypertrophic cardiomyopathy (HCM) is a primary cardiac disease transmitted as an autosomal dominant trait. Multiple chromosomal loci have been found to be involved in the etiology of this defect. LEOPARD syndrome is a genetic condition characteristically asso