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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Bibliografiska uppgifter
I publikationen:Meta Gene
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Elsevier 2015
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4561237/
https://ncbi.nlm.nih.gov/pubmed/26401487
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mgene.2015.07.010
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