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Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.
Jay PY, Harris BS, Maguire CT, Buerger A, Wakimoto H, Tanaka M, Kupershmidt S, Roden DM, Schultheiss TM, O'Brien TX, Gourdie RG, Berul CI, Izumo S. Jay PY, et al. Among authors: kupershmidt s. J Clin Invest. 2004 Apr;113(8):1130-7. doi: 10.1172/JCI19846. J Clin Invest. 2004. PMID: 15085192 Free PMC article.
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, Sawyer DB, Walter M, Li GH, Burgon PG, Maguire CT, Stapleton D, Schmitt JP, Guo XX, Pizard A, Kupershmidt S, Roden DM, Berul CI, Seidman CE, Seidman JG. Arad M, et al. Among authors: kupershmidt s. Circulation. 2003 Jun 10;107(22):2850-6. doi: 10.1161/01.CIR.0000075270.13497.2B. Epub 2003 Jun 2. Circulation. 2003. PMID: 12782567
From genes to channels: normal mechanisms.
Roden DM, Kupershmidt S. Roden DM, et al. Among authors: kupershmidt s. Cardiovasc Res. 1999 May;42(2):318-26. doi: 10.1016/s0008-6363(99)00063-2. Cardiovasc Res. 1999. PMID: 10533570 Review.
45 results