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Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families.
Amirian, Azam; Zafari, Zahra; Dalili, Mohammad; Saber, Siamak; Karimipoor, Morteza; Dabbagh Bagheri, Samira; Fazelifar, Amir Farjam; Zeinali, Sirous.
Afiliación
  • Amirian A; Biotechnology Research Center Pasteur Institute of Iran Tehran Iran.
  • 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.
  • Saber S; Cardiac Electrophysiology Research Center Rajaie Cardiovascular Medical, and Research Center Iran University of Medical Sciences Tehran Iran.
  • Karimipoor M; Biotechnology Research Center Pasteur Institute of Iran Tehran Iran.
  • Dabbagh Bagheri S; Medical Genetics Laboratory Kawsar Human Genetics Research Center Tehran Iran.
  • Fazelifar AF; 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.
J Arrhythm ; 34(3): 286-290, 2018 Jun.
Article en En | MEDLINE | ID: mdl-29951145
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: J Arrhythm Año: 2018 Tipo del documento: Article Pais de publicación: Japón
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: J Arrhythm Año: 2018 Tipo del documento: Article Pais de publicación: Japón