Haploinsufficiency of insulin gene enhancer protein 1 (ISL1) is associated with d-transposition of the great arteries

Congenital heart defects are the most common malformation, and are the foremost causes of mortality in the first year of life. Among congenital heart defects, conotruncal defects represent about 20% and are severe malformations with significant morbidity. Insulin gene enhancer protein 1 (ISL1) has b...

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Detalles Bibliográficos
Autores principales: Osoegawa, Kazutoyo, Schultz, Kathleen, Yun, Kenneth, Mohammed, Nebil, Shaw, Gary M, Lammer, Edward J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113275/
https://www.ncbi.nlm.nih.gov/pubmed/25077177
http://dx.doi.org/10.1002/mgg3.75

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113275/
https://www.ncbi.nlm.nih.gov/pubmed/25077177
http://dx.doi.org/10.1002/mgg3.75

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