Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance.

Liu, Hui-Ting; Ji, Fang-Fang; Wei, Ling; Zuo, An-Jun; Gao, Yu-Xiu; Qi, Lin; Jin, Bu; Wang, Ji-Gang; Zhao, Peng

Liu, Hui-Ting; Ji, Fang-Fang; Wei, Ling; Zuo, An-Jun; Gao, Yu-Xiu; Qi, Lin; Jin, Bu; Wang, Ji-Gang; Zhao, Peng.

Afiliación

Liu HT; Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China.
Ji FF; Department of Forensic Medicine, School of Basic Medicine, Qingdao University, Qingdao, Shandong 266071, China.
Wei L; Qingdao Sanatorium in Shandong Province, Qingdao, Shandong 266071, China.
Zuo AJ; Department of Internal Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China.
Gao YX; Department of Internal Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China.
Qi L; Department of Ultrasound, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China.
Jin B; Department of Forensic Medicine, School of Basic Medicine, Qingdao University, Qingdao, Shandong 266071, China.
Wang JG; Department of Forensic Medicine, School of Basic Medicine, Qingdao University, Qingdao, Shandong 266071, China.
Zhao P; Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China.

Chin Med J (Engl) ; 132(23): 2835-2841, 2019 Dec 05.

Article en En | MEDLINE | ID: mdl-31856055

Asunto(s)

Miosinas Cardíacas/genética; Cardiomiopatía Hipertrófica/genética; Mutación/genética; Cadenas Pesadas de Miosina/genética; Adolescente; Adulto; Biología Computacional; Exones/genética; Femenino; Humanos; Masculino; Persona de Mediana Edad; Linaje; Fenotipo; Análisis de Secuencia de ADN; Adulto Joven

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases / 6_other_circulatory_diseases Asunto principal: Cardiomiopatía Hipertrófica / Cadenas Pesadas de Miosina / Miosinas Cardíacas / Mutación Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Chin Med J (Engl) Año: 2019 Tipo del documento: Article País de afiliación: China

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