Exome Analysis of a Family with Wolff–Parkinson–White Syndrome Identifies a Novel Disease Locus

Wolff–Parkinson–White (WPW) syndrome is a common cause of supraventricular tachycardia that carries a risk of sudden cardiac death. To date, mutations in only one gene, PRKAG2, which encodes the 5’ -AMP-activated protein kinase subunit γ-2, have been identified as causative for WPW. DNA samples from...

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Dades bibliogràfiques
Publicat a:Am J Med Genet A
Autors principals: Bowles, Neil E., Jou, Chuanchau J., Arrington, Cammon B., Kennedy, Brett J., Earl, Aubree, Matsunami, Norisada, Meyers, Lindsay L., Etheridge, Susan P., Saarel, Elizabeth V., Bleyl, Steven B., Yost, H. Joseph, Yandell, Mark, Leppert, Mark F., Tristani-Firouzi, Martin, Gruber, Peter J.
Format: Artigo
Idioma:Inglês
Publicat: 2015
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4896306/
https://ncbi.nlm.nih.gov/pubmed/26284702
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37297
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