Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

Heterozygous mutations in NKX2.5, a homeobox transcription factor, were reported to cause secundum atrial septal defects and result in atrioventricular (AV) conduction block during postnatal life. To further characterize the role of NKX2.5 in cardiac morphogenesis, we sought additional mutations in...

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Autors principals: Benson, D. Woodrow, Silberbach, G. Michael, Kavanaugh-McHugh, Ann, Cottrill, Carol, Zhang, Yizhong, Riggs, Steve, Smalls, Octavia, Johnson, Mark C., Watson, Michael S., Seidman, J.G., Seidman, Christine E., Plowden, John, Kugler, John D.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 1999
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC409866/
https://ncbi.nlm.nih.gov/pubmed/10587520
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