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Progress in Biophysics and Molecular Biology|November 26, 2008
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndromeZahurul A Bhuiyan, Tarek S Momenah, Ahmad S Amin, et al.Pediatric Cardiology|February 3, 2009
Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?Zahurul A Bhuiyan, Safar Al-Shahrani, Ayman S Al-Khadra, et al.Pageof 2