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Journal Abstract Search

237 related items for PubMed ID: 15387941

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  • 2. [Family hypertrophic cardiomyopathy caused by a 14035c > t mutation in cardiac troponin T gene].
    Wang SX, Zou YB, Fu CY, Song L, Wang H, Wang JZ, Song XD, Chen JZ, Hui RT.
    Zhonghua Yi Xue Za Zhi; 2007 Feb 06; 87(6):371-4. PubMed ID: 17456375
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  • 4. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
    Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F.
    J Cardiovasc Med (Hagerstown); 2006 Aug 06; 7(8):601-7. PubMed ID: 16858239
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  • 11. Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.
    Mogensen J, Murphy RT, Kubo T, Bahl A, Moon JC, Klausen IC, Elliott PM, McKenna WJ.
    J Am Coll Cardiol; 2004 Dec 21; 44(12):2315-25. PubMed ID: 15607392
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  • 19. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.
    Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic BT, Ulmer HE, Kern M, Katus HA, Frey N.
    Cardiovasc Res; 2010 Jun 01; 86(3):452-60. PubMed ID: 20083571
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  • 20. [Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families].
    Fan XP, Yang ZW, Feng XL, Yang FH, Xiao B, Liang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 01; 28(4):387-92. PubMed ID: 21811976
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