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Query Trace: Romano-Ward Syndrome and KCNQ1[original query]

KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1. American journal of medical genetics. Part A 2016 Apr . Vyas Bijal, Puri Ratna D, Namboodiri Narayanan, Nair Mohan, Sharma Deepak, Movva Sireesha, Saxena Renu, Bohora Shomu, Aggarwal Neeraj, Vora Amit, Kumar Jatinder, Singh Tarandeep, Verma Ishwar Similar articles in PubMed
Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers. Scandinavian journal of clinical and laboratory investigation 2008 68 (5): 362-8. Berge K E, Haugaa K H, Früh A, Anfinsen O-G, Gjesdal K, Siem G, Oyen N, Greve G, Carlsson A, Rognum T O, Hallerud M, Kongsgård E, Amlie J P, Leren T Similar articles in PubMed
Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome. Frontiers of medicine in China 2007 Jul 1 (3): 312-5. Du Rong, Tian Li, Yuan Guohui, Li Jin, Ren Faxin, Gui Le, Li Wei, Zhang Shouyan, Kang Cailian, Yang Jung Similar articles in PubMed