TY  - GEN
AU  - Okada,T
AU  - Shiono,Y
AU  - Hayashi,H
AU  - Satoh,H
AU  - Sawada,T
AU  - Suzuki,A
AU  - Takeda,Y
AU  - Yano,M
AU  - Michitaka,K
AU  - Onji,M
AU  - Mabuchi,H
TI  - Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease
SN  - 1059-7794
PY  - 2000///0531
KW  - Adenosine Triphosphatases
KW  - genetics
KW  - Amino Acid Substitution
KW  - Asian People
KW  - Carrier Proteins
KW  - Cation Transport Proteins
KW  - Ceruloplasmin
KW  - analysis
KW  - Copper
KW  - blood
KW  - Copper-Transporting ATPases
KW  - DNA Mutational Analysis
KW  - DNA Transposable Elements
KW  - Female
KW  - Frameshift Mutation
KW  - Genotype
KW  - Geography
KW  - Hepatolenticular Degeneration
KW  - Humans
KW  - Japan
KW  - Male
KW  - Mutation
KW  - Mutation, Missense
KW  - Pedigree
KW  - Phenotype
KW  - Polymerase Chain Reaction
KW  - Polymorphism, Single-Stranded Conformational
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/(SICI)1098-1004(200005)15:5<454::AID-HUMU7>3.0.CO;2-J
ER  -