A clinical and Molecular Genetic Study on Egyptian Children with Hypertrophic Cardiomyopathy
Arwa Ahmed El-Darsh;
Abstract
Hypertrophic cardiomyopathy (HCM) is a primary genetic disease of the myocardium characterized by hypertrophy of left ventricle and interventricular septum and inherited in an autosomal dominant fashion. It is one of the leading causes of sudden cardiac d
Other data
| Title | A clinical and Molecular Genetic Study on Egyptian Children with Hypertrophic Cardiomyopathy | Other Titles | دراسة وراثية إكلينيكية وجزيئية على أطفال مصريين مصابين بضعف تضخمي في عضلة القلب | Authors | Arwa Ahmed El-Darsh | Keywords | A clinical and Molecular Genetic Study on Egyptian Children with Hypertrophic Cardiomyopathy | Issue Date | 2010 | Description | Hypertrophic cardiomyopathy (HCM) is a primary genetic disease of the myocardium characterized by hypertrophy of left ventricle and interventricular septum and inherited in an autosomal dominant fashion. It is one of the leading causes of sudden cardiac d |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 99631r3539.pdf | 228.84 kB | Adobe PDF | View/Open |
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