Last Posted: Jul 14, 2015
- H558R polymorphism in SCN5A is associated with Keshan disease and QRS prolongation in Keshan disease patients.
Jiang S, et al. Genetics and molecular research : GMR 2014 0 (3) 6569-76
- Analysis of glutathione peroxidase 1 gene polymorphism and Keshan disease in Heilongjiang Province, China.
Wei H L, et al. Genetics and molecular research : GMR 2011 0 (4) 2996-3001
- Keshan disease
From NCATS Genetic and Rare Diseases Information Center
- [Polymorphisms in the glutathione peroxidase-1 gene associated with increased risk of Keshan disease].
Lei Cong, et al. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2010 7 (7) 617-21
- Interaction of glutathione peroxidase-1 and selenium in endemic dilated cardiomyopathy.
Lei Cong, et al. Clinica chimica acta; international journal of clinical chemistry 2009 1 (1-2) 102-8
- [The study on relation of HLA-DRB1 gene polymorphism to Keshan disease and its association and linkage in the core families].
Wei Jin, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2007 2 (1) 91-3
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
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- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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