Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy. [electronic resource]
Producer: 20030409Description: 981-6 p. digitalISSN:- 0735-1097
- Adolescent
- Adult
- Aged
- Cardiomyopathy, Hypertrophic, Familial -- complications
- Child
- Chromosome Mapping
- Death, Sudden, Cardiac -- etiology
- Drosophila Proteins
- Female
- Humans
- Male
- Middle Aged
- Mutation, Missense -- genetics
- Pedigree
- Polymorphism, Single-Stranded Conformational
- Sequence Analysis
- Tropomyosin -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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