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NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity
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 hypothesized that s...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4351524/ https://ncbi.nlm.nih.gov/pubmed/25742962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep08848 |
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