Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the Oguchi form of congenital stationary night blindness

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 6, 1998, Pages 2824-2827

  Khani, Shahrokh C ^a   Nielsen, Lori ^a   Vogt, Todd M ^a  

^a UNIVERSITY AT BUFFALO   (United States)

Author keywords

Isoprenylation human; Phototransduction; Retina; Retinopathy

Indexed keywords

ASPARTIC ACID; MUTANT PROTEIN; POLYPEPTIDE; PROTEIN KINASE; RHODOPSIN; RHODOPSIN KINASE; UNCLASSIFIED DRUG; VALINE;

ANIMAL CELL; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CATALYSIS; CONGENITAL DISORDER; CONTROLLED STUDY; EXON; GENE DELETION; MUTATION; NIGHT BLINDNESS; NONHUMAN; PATHOGENICITY; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION;

AMINO ACID SEQUENCE; ANIMALS; COS CELLS; EYE PROTEINS; HUMANS; LIGHT; MOLECULAR SEQUENCE DATA; MUTATION; NIGHT BLINDNESS; PHOSPHORYLATION; PROTEIN KINASES; RECOMBINANT PROTEINS; RHODOPSIN; RHODOPSIN KINASE; SEQUENCE HOMOLOGY, AMINO ACID;

ANIMALIA; GENETTA;

EID: 0032539806     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.6.2824     Document Type: Article

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