Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Romano-Ward Syndrome and KCNQ1[original query] |
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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 |
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 |
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 |
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