A Complete Absence of Missense Mutation in Myosin Regulatory and Essential Light Chain Genes of South Indian Hypertrophic and Dilated Cardiomyopathies.

Rani, Deepa Selvi; Nallari, Pratibha; Rani, Jhansi; Nizamuddin, Sheikh; Seelamneni, Thulasamma; Narasimhan, Calambur; Thangaraj, Kumarasamy

Rani, Deepa Selvi; Nallari, Pratibha; Rani, Jhansi; Nizamuddin, Sheikh; Seelamneni, Thulasamma; Narasimhan, Calambur; Thangaraj, Kumarasamy.

Afiliación

Rani DS; CSIR - Centre for Cellular and Molecular Biology (CCMB), Hyderabad, India.
Nallari P; Department of Genetics, Osmania University, Hyderabad, India.
Rani J; CSIR - Centre for Cellular and Molecular Biology (CCMB), Hyderabad, India.
Nizamuddin S; CSIR - Centre for Cellular and Molecular Biology (CCMB), Hyderabad, India.
Seelamneni T; CSIR - Centre for Cellular and Molecular Biology (CCMB), Hyderabad, India.
Narasimhan C; Department of Cardiology, CARE Hospitals, Hyderabad, India.
Thangaraj K; CSIR - Centre for Cellular and Molecular Biology (CCMB), Hyderabad, India, thangs@ccmb.res.in.

Cardiology ; 141(3): 156-166, 2018.

Article en En | MEDLINE | ID: mdl-30605904

Asunto(s)

Miosinas Cardíacas/genética; Cardiomiopatía Dilatada/genética; Cardiomiopatía Hipertrófica/genética; Mutación Missense; Cadenas Ligeras de Miosina/genética; Adulto; Estudios de Casos y Controles; Humanos; India; Persona de Mediana Edad; Linaje; Fenotipo

Palabras clave

Indian cardiomyopathies; MYL2; MYL3; Mutations; Sarcomeric genes

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cardiomiopatía Hipertrófica / Cardiomiopatía Dilatada / Cadenas Ligeras de Miosina / Mutación Missense / Miosinas Cardíacas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Humans / Middle aged País/Región como asunto: Asia Idioma: En Año: 2018 Tipo del documento: Article

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