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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Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1999
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC409866/
https://ncbi.nlm.nih.gov/pubmed/10587520
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