Mutational screening of exon 1 of smad7 in Malay patients with ventricular septal defect
Congenital heart disease (CHD) affects approximately 8 in every 1000 live births with ventricular septal defect (VSD) being the most common phenotype. VSD is thought to arise from genetics and environmental factors, however most of the causes remain unknown. It was hypothesized that SMAD7 gene co...
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| Main Author: | |
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| Format: | Thesis |
| Language: | English |
| Published: |
2015
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| Subjects: | |
| Online Access: | http://eprints.usm.my/39777/1/Dr_Hashima_Hashim_%28Medical_Genetics%29-24_pages.pdf |
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