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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Bibliographische Detailangaben
Veröffentlicht in:Congenit Heart Dis
Hauptverfasser: Ellesøe, Sabrina Gade, Johansen, Morten Munk, Bjerre, Jesper Vandborg, Hjortdal, Vibeke Elisabeth, Brunak, Søren, Larsen, Lars Allan
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2015
Schlagworte:
Education Forum
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5019245/
https://ncbi.nlm.nih.gov/pubmed/26679770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/chd.12317
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