These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
56 related articles for article (PubMed ID: 9503863)
21. A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome. Krahn AD; Wang J; Spindler B; Skanes AC; Yee R; Klein GJ; Hegele RA Am Heart J; 2000 Jul; 140(1):146-9. PubMed ID: 10874277 [TBL] [Abstract][Full Text] [Related]
23. Letter by Kaufman regarding article, "Closer look at genetic testing in long-QT syndrome: will DNA diagnostics ever be enough?". Kaufman ES Circulation; 2010 Jun; 121(23):e439; author reply e440. PubMed ID: 20547937 [No Abstract] [Full Text] [Related]
30. Searching for a Rosetta Stone: genetic data and clinical patient management. Triedman JK; MacRae C Heart Rhythm; 2014 Oct; 11(10):1714-5. PubMed ID: 25046859 [No Abstract] [Full Text] [Related]
31. Long QT and Harvey-ras. Jeffery S; Jamieson R; Patton MA; Till J Lancet; 1992 Jan; 339(8787):255. PubMed ID: 1346223 [No Abstract] [Full Text] [Related]
32. Targeting sigma receptor 1 in long QT syndrome. Crunkhorn S Nat Rev Drug Discov; 2022 Apr; 21(4):260. PubMed ID: 35228714 [No Abstract] [Full Text] [Related]
33. DNA structural variants as genetic risk factors for the long QT syndrome. Rich SS; Hall IM J Am Coll Cardiol; 2011 Jan; 57(1):48-50. PubMed ID: 21185500 [No Abstract] [Full Text] [Related]
34. Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population. Iwasa H; Itoh T; Nagai R; Nakamura Y; Tanaka T J Hum Genet; 2000; 45(3):182-3. PubMed ID: 10807545 [TBL] [Abstract][Full Text] [Related]
35. Exclusion of HRAS from long QT locus. Roy N; Kahlem P; Dausse E; Bennaceur M; Fauré S; Weissenbach J; Komajda M; Denjoy I; Coumel P; Schwartz K Nat Genet; 1994 Oct; 8(2):113-4. PubMed ID: 7842005 [No Abstract] [Full Text] [Related]