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AMPD1基因的常见变异预测心力衰竭患者的临床结果有所改善

E Loh1, T R Rebbeck, P D Mahoney

  • 1Cardiovascular Division, Department of Medicine, Biostatistics and Epidemiology, Hospital of the University of Pennsylvania, University of Pennsylvania, Philadelphia, PA 19104, USA. lohe@mail.med.upenn.edu

Circulation
|March 23, 1999
PubMed
概括

在充血性心力衰竭 (CHF) 患者中,继承一个突变的腺单酸脱氨酶 (AMPD1) 基因组与没有心脏移植的更长的存活时间有关. 这种遗传因素可能会影响心力衰竭的结果.

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