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Mutational analysis of SCN5A gene in long QT syndrome.
Qureshi, Sameera Fatima; Ali, Altaf; John, Princy; Jadhav, Amol P; Venkateshwari, Ananthapur; Rao, Hygriv; Jayakrishnan, M P; Narasimhan, Calambur; Shenthar, Jayaprakash; Thangaraj, Kumarasamy; Nallari, Pratibha.
Afiliação
  • Qureshi SF; Dept. of Genetics, University College of Science, Osmania University, Hyderabad 500007, Andhra Pradesh, India.
  • Ali A; Dept. of Genetics, University College of Science, Osmania University, Hyderabad 500007, Andhra Pradesh, India.
  • John P; Dept. of Genetics, University College of Science, Osmania University, Hyderabad 500007, Andhra Pradesh, India.
  • Jadhav AP; Dept. of Genetics, University College of Science, Osmania University, Hyderabad 500007, Andhra Pradesh, India.
  • Venkateshwari A; Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad 500016, Andhra Pradesh, India.
  • Rao H; Krishna Institute of Medical Sciences, 1-8-31/1, Minister Road, Secunderabad 500 003, Andhra Pradesh, India.
  • Jayakrishnan MP; Institute of Maternal and Child Health, Calicut Medical College, Calicut 8, Kerala, India.
  • Narasimhan C; Care Hospital, Hyderabad, Andhra Pradesh, India.
  • Shenthar J; Sri Jayadeva Institute of Cardiovascular Science and Research, Jayanagar 9th Block, Bannerghatta Road, Bangalore 560069, Karnataka, India.
  • Thangaraj K; Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500 007, Andhra Pradesh, India.
  • Nallari P; Dept. of Genetics, University College of Science, Osmania University, Hyderabad 500007, Andhra Pradesh, India.
Meta Gene ; 6: 26-35, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26401487

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article