Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2‐5 Mutation and a Review of the Literature

OBJECTIVE: Atrial septal defect (ASD) is the second most common congenital heart defect (CHD) and is observed in families as an autosomal dominant trait as well as in nonfamilial CHD. Mutations in the NKX2‐5 gene, located on chromosome 5, are associated with ASD, often combined with conduction distu...

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Detalles Bibliográficos
Autores principales: Ellesøe, Sabrina Gade, Johansen, Morten Munk, Bjerre, Jesper Vandborg, Hjortdal, Vibeke Elisabeth, Brunak, Søren, Larsen, Lars Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Education Forum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019245/
https://www.ncbi.nlm.nih.gov/pubmed/26679770
http://dx.doi.org/10.1111/chd.12317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019245/
https://www.ncbi.nlm.nih.gov/pubmed/26679770
http://dx.doi.org/10.1111/chd.12317

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