Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease / 대한간학회지
The Korean Journal of Hepatology
;
: 295-298, 2009.
Article
in Korean
| WPRIM
| ID: wpr-181189
ABSTRACT
No abstract available.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Haplotypes
/
Adenosine Triphosphatases
/
Amino Acid Substitution
/
Cation Transport Proteins
/
Republic of Korea
/
Genotype
/
Hepatolenticular Degeneration
/
Mutation
Limits:
Humans
Country/Region as subject:
Asia
Language:
Korean
Journal:
The Korean Journal of Hepatology
Year:
2009
Type:
Article
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