Novel Clinical Manifestation of the Known SCN5A D1790G Mutation.

Blich, Miry; Efrati, Edna; Marai, Ibrahim; Suleiman, Mahmoud; Gepstein, Lior; Boulous, Monther

Blich, Miry; Efrati, Edna; Marai, Ibrahim; Suleiman, Mahmoud; Gepstein, Lior; Boulous, Monther.

Affiliation

Blich M; Division of Pacing and Electrophysiology, Rambam Health Care Campus, Haifa, Israel.

Cardiology ; 132(4): 228-32, 2015.

Article in En | MEDLINE | ID: mdl-26304620

Subject(s)

Brugada Syndrome/genetics; Long QT Syndrome/genetics; NAV1.5 Voltage-Gated Sodium Channel/genetics; Cardiac Conduction System Disease; Electrocardiography, Ambulatory; Genetic Testing; Humans; Male; Middle Aged; Mutation, Missense; Sodium/blood

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / Brugada Syndrome / NAV1.5 Voltage-Gated Sodium Channel Type of study: Prognostic_studies Limits: Humans / Male / Middle aged Language: En Journal: Cardiology Year: 2015 Type: Article Affiliation country: Israel

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