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Cardiovascular defects in a mouse model of HOXA1 syndrome
Congenital heart disease is one of the most common human birth defects, yet many genes and pathways regulating heart development remain unknown. A recent study in humans revealed that mutations in a single Hox gene, HOXA1 (Athabascan Brainstem Dysgenesis Syndrome, Bosley-Salih-Alorainy Syndrome), ca...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3235008/ https://ncbi.nlm.nih.gov/pubmed/21940751 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr434 |
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