Mutational analysis of SCN5A gene in long QT syndrome

The SCN5A gene encodes for the INa channel implicated in long QT syndrome type-3 (LQTS-type-3). Clinical symptoms of this type are lethal as most patients had a sudden death during sleep. Screening of SCN5A in South Indian cohort by PCR-SSCP analyses revealed five polymorphisms — A29A (exon-2), H558...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4561237/
https://www.ncbi.nlm.nih.gov/pubmed/26401487
http://dx.doi.org/10.1016/j.mgene.2015.07.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4561237/
https://www.ncbi.nlm.nih.gov/pubmed/26401487
http://dx.doi.org/10.1016/j.mgene.2015.07.010

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