NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity
Abstract NKX2-5 mutations are associated with different forms of congenital heart disease. Despite the knowledge gained from molecular and animal studies, genotype-phenotype correlations in humans are limited by the lack of large cohorts and the incomplete assessment of family members. We hypothesiz...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | İngilizce |
| Baskı/Yayın Bilgisi: |
2015
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| Online Erişim: | https://doi.org/10.1038/srep08848 https://www.nature.com/articles/srep08848.pdf |
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