TY  - GEN
AU  - Forbes,J R
AU  - Cox,D W
TI  - Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?
SN  - 0002-9297
PY  - 1999///0201
KW  - Adenosine Triphosphatases
KW  - chemistry
KW  - Apoenzymes
KW  - metabolism
KW  - Biological Transport
KW  - Carrier Proteins
KW  - Cation Transport Proteins
KW  - Cell Division
KW  - Ceruloplasmin
KW  - Copper
KW  - Copper Transport Proteins
KW  - Copper-Transporting ATPases
KW  - Cysteine
KW  - genetics
KW  - DNA, Complementary
KW  - Fungal Proteins
KW  - Genetic Complementation Test
KW  - Hepatolenticular Degeneration
KW  - enzymology
KW  - Humans
KW  - Immune Sera
KW  - Iron
KW  - Mutagenesis, Site-Directed
KW  - Mutation, Missense
KW  - Phenotype
KW  - Recombinant Fusion Proteins
KW  - immunology
KW  - Saccharomyces cerevisiae
KW  - Saccharomyces cerevisiae Proteins
KW  - Temperature
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1086/302163
ER  -