GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

Congenital heart diseases (CHD) occur in nearly 1% of all live births and are the major cause of infant mortality and morbidity. Although an improved understanding of the genetic causes of CHD would provide insight into the underlying pathobiology, the genetic etiology of most CHD remains unknown. H...

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Detalhes bibliográficos
Main Authors: Kodo, Kazuki, Nishizawa, Tsutomu, Furutani, Michiko, Arai, Shoichi, Yamamura, Eiji, Joo, Kunitaka, Takahashi, Takao, Matsuoka, Rumiko, Yamagishi, Hiroyuki
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2009
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2728998/
https://ncbi.nlm.nih.gov/pubmed/19666519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0904744106
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