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Sudden infant death syndrome in mice with an inherited mutation in RyR2.
Mathur N, Sood S, Wang S, van Oort RJ, Sarma S, Li N, Skapura DG, Bayle JH, Valderrábano M, Wehrens XH. Mathur N, et al. Among authors: sood s. Circ Arrhythm Electrophysiol. 2009 Dec;2(6):677-85. doi: 10.1161/CIRCEP.109.894683. Circ Arrhythm Electrophysiol. 2009. PMID: 20009080 Free PMC article.
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy.
Kannankeril PJ, Mitchell BM, Goonasekera SA, Chelu MG, Zhang W, Sood S, Kearney DL, Danila CI, De Biasi M, Wehrens XH, Pautler RG, Roden DM, Taffet GE, Dirksen RT, Anderson ME, Hamilton SL. Kannankeril PJ, et al. Among authors: sood s. Proc Natl Acad Sci U S A. 2006 Aug 8;103(32):12179-84. doi: 10.1073/pnas.0600268103. Epub 2006 Jul 27. Proc Natl Acad Sci U S A. 2006. PMID: 16873551 Free PMC article.
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
Lalani SR, Thakuria JV, Cox GF, Wang X, Bi W, Bray MS, Shaw C, Cheung SW, Chinault AC, Boggs BA, Ou Z, Brundage EK, Lupski JR, Gentile J, Waisbren S, Pursley A, Ma L, Khajavi M, Zapata G, Friedman R, Kim JJ, Towbin JA, Stankiewicz P, Schnittger S, Hansmann I, Ai T, Sood S, Wehrens XH, Martin JF, Belmont JW, Potocki L. Lalani SR, et al. Among authors: sood s. J Med Genet. 2009 Mar;46(3):168-75. doi: 10.1136/jmg.2008.061002. Epub 2008 Sep 23. J Med Genet. 2009. PMID: 18812404 Free PMC article.
1,603 results