Dilative cardiomyopathy: Genetic and clinical contributions in a family study
β Scribed by A. Sciacca; S. Villatico Campbell; F. Di Maio; A. Sciarra; P. Grammatico; G. Del Porto
- Book ID
- 119441109
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 81 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0022-2828
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
We compared clinical data from two related Chinese patients with fatal familial insomnia (FFI) and collected information about their pedigree. The clinical features in the two cases were similar and included initial progressive insomnia and sympathetic activation, which persisted throughout the clin
## Abstract A novel __SPG4__ 906delT frameβshift mutation in exon 6 was identified in a large Italian family with an autosomal dominant form of hereditary spastic paraplegia (ADHSP). Intrafamilial phenotypic variations observed in the pedigree included spasticity and additional clinical features, s
A candidate gene (HFE) has been described for hereditary hemochromatosis on chromosome 6. The study of well-defined atypical hemochromatosis families using genetic markers may increase our understanding of the sensitivity and the specificity of genotyping in hemochromatosis. One hundred and thirteen