Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families.

Zafari, Zahra; Dalili, Mohammad; Zeinali, Sirus; Saber, Siamak; Fazeli Far, Amir Farjam; Akbari, Mohammad Taghi

Zafari, Zahra; Dalili, Mohammad; Zeinali, Sirus; Saber, Siamak; Fazeli Far, Amir Farjam; Akbari, Mohammad Taghi.

Afiliación

Zafari Z; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Dalili M; Cardiac Electrophysiology Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
Zeinali S; Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Saber S; Cardiac Electrophysiology Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
Fazeli Far AF; Cardiac Electrophysiology Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
Akbari MT; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. Electronic address: mtakbari@modares.ac.ir.

J Electrocardiol ; 50(6): 912-918, 2017.

Article en En | MEDLINE | ID: mdl-29033053

Asunto(s)

Canal de Potasio KCNQ1/genética; Mutación/genética; Síndrome de Romano-Ward/genética; Niño; Electrocardiografía; Femenino; Pruebas Genéticas; Humanos; Irán; Masculino; Linaje; Análisis de Secuencia de ADN

Palabras clave

Arrhythmia; Founder mutation; Genetic testing; Iran; LQTS; Next generation sequencing

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Romano-Ward / Canal de Potasio KCNQ1 / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: J Electrocardiol Año: 2017 Tipo del documento: Article País de afiliación: Irán

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