Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes.

Lin, Yubi; Zhao, Ting; He, Siqi; Huang, Jiana; Liu, Qianru; Yang, Zhe; Qin, Jiading; Yu, Nan; Lu, Hongyun; Lin, Xiufang

Lin, Yubi; Zhao, Ting; He, Siqi; Huang, Jiana; Liu, Qianru; Yang, Zhe; Qin, Jiading; Yu, Nan; Lu, Hongyun; Lin, Xiufang.

Afiliación

Lin Y; Department of Cardiology and Cardiovascular Intervention, Interventional Medical Center, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Zhao T; Guangdong Provincial Key Laboratory of Biomedical Imaging and Guangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.
He S; Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangdong Cardiovascular Institute, Guangdong Geriatrics Institute, Guangzhou, China.
Huang J; Department of Cardiology and Cardiovascular Intervention, Interventional Medical Center, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Liu Q; The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Yang Z; The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Qin J; Jinan University, Guangzhou, China.
Yu N; Department of Cardiology and Cardiovascular Intervention, Interventional Medical Center, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Lu H; Department of Cardiology and Cardiovascular Intervention, Interventional Medical Center, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Lin X; Department of Clinical Laboratory, Zhujiang Hospital of Southern Medical University, Guangzhou, China.

Ann Noninvasive Electrocardiol ; 25(1): e12694, 2020 01.

Article en En | MEDLINE | ID: mdl-31565860

Asunto(s)

Muerte Súbita; Secuenciación del Exoma/métodos; Predisposición Genética a la Enfermedad/genética; Canal de Potasio KCNQ1/genética; Síndrome de QT Prolongado/genética; Mutación/genética; Femenino; Humanos; Persona de Mediana Edad

Palabras clave

KCNQ1; genetics; long QT syndrome; sudden death

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Predisposición Genética a la Enfermedad / Muerte Súbita / Canal de Potasio KCNQ1 / Secuenciación del Exoma / Mutación Tipo de estudio: Prognostic_studies Límite: Female / Humans / Middle aged Idioma: En Revista: Ann Noninvasive Electrocardiol Asunto de la revista: CARDIOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

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