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192 related items for PubMed ID: 8989109

  • 1. Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy.
    Forissier JF, Carrier L, Farza H, Bonne G, Bercovici J, Richard P, Hainque B, Townsend PJ, Yacoub MH, Fauré S, Dubourg O, Millaire A, Hagège AA, Desnos M, Komajda M, Schwartz K.
    Circulation; 1996 Dec 15; 94(12):3069-73. PubMed ID: 8989109
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  • 2. A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy.
    Gerull B, Osterziel KJ, Witt C, Dietz R, Thierfelder L.
    Hum Mutat; 1998 Dec 15; 11(2):179-82. PubMed ID: 9482583
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  • 3. Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.
    Posen BM, Moolman JC, Corfield VA, Brink PA.
    Br Heart J; 1995 Jul 15; 74(1):40-6. PubMed ID: 7662452
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  • 4. Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis.
    Anan R, Shono H, Kisanuki A, Arima S, Nakao S, Tanaka H.
    Circulation; 1998 Aug 04; 98(5):391-7. PubMed ID: 9714088
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  • 5. Sudden death due to troponin T mutations.
    Moolman JC, Corfield VA, Posen B, Ngumbela K, Seidman C, Brink PA, Watkins H.
    J Am Coll Cardiol; 1997 Mar 01; 29(3):549-55. PubMed ID: 9060892
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  • 6. [A novel missense mutation, K124N, in the troponin T gene of Chinese populations with hypertrophic cardiomyopathy].
    An FS, Zhang Y, Li DQ, Yang XS, Li L, Zhang C, Yan ML, Wang Y, An GP.
    Zhonghua Yi Xue Za Zhi; 2004 Aug 17; 84(16):1340-3. PubMed ID: 15387941
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  • 7. Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy.
    Nakajima-Taniguchi C, Matsui H, Fujio Y, Nagata S, Kishimoto T, Yamauchi-Takihara K.
    J Mol Cell Cardiol; 1997 Feb 17; 29(2):839-43. PubMed ID: 9140840
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  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.
    Dausse E, Komajda M, Fetler L, Dubourg O, Dufour C, Carrier L, Wisnewsky C, Bercovici J, Hengstenberg C, al-Mahdawi S.
    J Clin Invest; 1993 Dec 06; 92(6):2807-13. PubMed ID: 8254035
    [Abstract] [Full Text] [Related]

  • 10. Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients.
    García-Castro M, Reguero JR, Batalla A, Díaz-Molina B, González P, Alvarez V, Cortina A, Cubero GI, Coto E.
    Clin Chem; 2003 Aug 06; 49(8):1279-85. PubMed ID: 12881443
    [Abstract] [Full Text] [Related]

  • 11. Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failure.
    Ko YL, Chen JJ, Tang TK, Cheng JJ, Lin SY, Liou YC, Kuan P, Wu CW, Lien WP, Liew CC.
    Hum Genet; 1996 May 06; 97(5):585-90. PubMed ID: 8655135
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  • 18. Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.
    Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B.
    J Mol Med (Berl); 1998 Mar 06; 76(3-4):208-14. PubMed ID: 9535554
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  • 20. Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan.
    Chiou KR, Chu CT, Charng MJ.
    J Cardiol; 2015 Mar 06; 65(3):250-6. PubMed ID: 25086479
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