Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease.
10.3350/kjhep.2009.15.3.295
- Author:
Hyun Seok JIN
1
;
Bermseok OH
Author Information
1. Department of Biomedical Engineering, School of Medicine, Kyung Hee University, Seoul, Korea. ohbs@khu.ac.kr
- Publication Type:Editorial ; Comment
- Keywords:
Genetic metabolic disorder;
Wilson disease;
ATP7B;
Haplotype
- MeSH:
Adenosine Triphosphatases/*genetics;
Amino Acid Substitution;
Cation Transport Proteins/*genetics;
Genotype;
Haplotypes;
Hepatolenticular Degeneration/diagnosis/*genetics;
Humans;
Mutation;
Republic of Korea
- From:The Korean Journal of Hepatology
2009;15(3):295-298
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
No abstract available.
