Novel mutations of KCNQ1 in Long QT syndrome

BACKGROUND: Autosomal recessive Long QT syndrome is characterized by prolonged QTc along with congenital bilateral deafness depends on mutations in K(+) channel genes. A family of a Long QT syndrome proband from India has been identified with novel indel variations. METHODS: The molecular study of t...

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Detalhes bibliográficos
Main Authors: Qureshi, Sameera F., Ali, Altaf, Ananthapur, Venkateshwari, Jayakrishnan, M.P., Calambur, Narasimhan, Thangaraj, Kumarasamy, Nallari, Pratibha
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2013
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3861163/
https://ncbi.nlm.nih.gov/pubmed/24206879
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ihj.2013.08.025
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