Novel mutations of KCNQ1 in Long QT syndrome

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 the...

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Bibliographic Details
Main Authors: Sameera F. Qureshi, Altaf Ali, Venkateshwari Ananthapur, M.P. Jayakrishnan, Narasimhan Calambur, Kumarasamy Thangaraj, Pratibha Nallari
Format: Article
Language:English
Published: Elsevier 2013-09-01
Series:Indian Heart Journal
Subjects:
Long QT syndrome
JLN syndrome
3D KCNQ1 structure
Novel mutations
Family study
Online Access:http://www.sciencedirect.com/science/article/pii/S0019483213002551

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http://www.sciencedirect.com/science/article/pii/S0019483213002551

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