DELETERIOUS MUTATIONS IN SCN10A ARE ASSOCIATED WITH LONG QT SYNDROME

In silico analysis, tissue-specific expression, and review of public genetic databases were performed in search for damaging mutations. 2,000 control exomes were also used for allele frequencies.

Bibliographische Detailangaben

Veröffentlicht in:	Journal of the American College of Cardiology 2017-03, Vol.69 (11), p.509-509
Hauptverfasser:	Ziki, Maen D. Abou, Seidelmann, Sara, Smith, Emily, Narayanan, Anand, Atteya, Gourg, Jiang, Yuexin, Gil-Fernandez, Rodolfo, Marieb, Mark, Akar, Joseph, Mani, Arya
Format:	Artikel
Sprache:	eng
Schlagworte:	Cardiology Cardiovascular Internal Medicine Long QT syndrome Mutation Sodium
Online-Zugang:	Volltext
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