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心血管病与基因突变 (1)家族性肥厚型心肌病和扩张型心肌病与基因突变 被引量:2

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作者 陈在嘉
机构地区 中国医学科学院
出处 《中国循环杂志》 CSCD 北大核心 1999年第3期130-131,共2页 Chinese Circulation Journal
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  • 1Morales A, Hershberger RE.Genetic evaluation of dilated cardiomyopathy. Curr Cardiol Rep, 2013, 15: 1-8.
  • 2Mestroni L, Maisch B, McKenna WJ, et al. Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy. Eur Heart J, 1999, 20: 93-102.
  • 3Fatkin D. Guidelines for the diagnosis and management of familial dilated cardiomyopathy. Heart Lung Circ, 2011, 20: 691-693.
  • 4Hershberger RE, Siegfried JD. Update 2011: clinical and genetic issues in familial dilated cardiomyopathy. J Am Coil Cardiol, 2011, 57: 1641-1649.
  • 5Herman DS, Lam L, Taylor MR, et al.Truncations of titin causing dilated cardiomyopathy. N Engl J Med, 2012, 366: 619-628.
  • 6Gun W, Bharmal S J, Esbona K, et al. Titin diversity-alternative splicing gone wild. J Bimned Biotechnol, 2010, 2010: 753675.
  • 7Chauveau C, Bonnemann CG, Julien C, et al. Recessive TTN truncating mutations define novel forms of core myopathy with heart disease. Hum Mol Genet, 2014, 23: 980-991.
  • 8Voelke| T, Linke WA. Conformation-regulated mechanosensory control via titin domains in cardiac muscle. Pflugers Arch, 2011,462: 143-154.
  • 9Greaser ML. Stressing the giant: a new approach to understanding dilated eardiomyopathy. J Mol Cell Cardiol, 2009, 47: 347-349.
  • 10Braueh KM, Karst ML, Herron KJ, et al. Mutations in ribonucleie acid binding protein gene cause familial dilated eardiomyopathy. J Am Coll Cardiol, 2009, 54: 930-941.

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