Korean J Hepatol.  2009 Sep;15(3):295-298. 10.3350/kjhep.2009.15.3.295.

Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease

Affiliations
  • 1Department of Biomedical Engineering, School of Medicine, Kyung Hee University, Seoul, Korea. ohbs@khu.ac.kr

Abstract

No abstract available.

Keyword

Genetic metabolic disorder; Wilson disease; ATP7B; Haplotype

MeSH Terms

Adenosine Triphosphatases/*genetics
Amino Acid Substitution
Cation Transport Proteins/*genetics
Genotype
Haplotypes
Hepatolenticular Degeneration/diagnosis/*genetics
Humans
Mutation
Republic of Korea
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