TY  - GEN
AU  - Wilkie,S E
AU  - Li,Y
AU  - Deery,E C
AU  - Newbold,R J
AU  - Garibaldi,D
AU  - Bateman,J B
AU  - Zhang,H
AU  - Lin,W
AU  - Zack,D J
AU  - Bhattacharya,S S
AU  - Warren,M J
AU  - Hunt,D M
AU  - Zhang,K
TI  - Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy
SN  - 0002-9297
PY  - 2001///0906
KW  - Amino Acid Sequence
KW  - Amino Acid Substitution
KW  - Calcium-Binding Proteins
KW  - chemistry
KW  - Corneal Dystrophies, Hereditary
KW  - genetics
KW  - DNA
KW  - analysis
KW  - Female
KW  - Glutamic Acid
KW  - Glycine
KW  - Guanylate Cyclase-Activating Proteins
KW  - Humans
KW  - Male
KW  - Models, Molecular
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Pedigree
KW  - Protein Conformation
KW  - Pyrimidines
KW  - Sequence Homology, Amino Acid
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/323265
ER  -