The spectrum of human rhodopsin disease mutations through the lens of interspecific variation

Gene

Volumn 332, Issue 1-2, 2004, Pages 107-118

  Briscoe, Adriana D ^a   Gaur, Charu ^b   Kumar, Sudhir ^b,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b ARIZONA STATE UNIVERSITY   (United States)

^c ARIZONA STATE UNIVERSITY   (United States)

Author keywords

ADRP; ARRP; autosomal dominant retinitis pigmentosa; electroretinogram; ERG; maximum likelihood; maximum parsimony; ML; MP; neighbor joining; Neutral theory; NJ; Opsin; Photoreceptor; retinitis pigmentosa; Retinitis pigmentosa; RP; Visual pigment

Indexed keywords

AMINO ACID DERIVATIVE; RHODOPSIN;

AMINO ACID SEQUENCE; ARTICLE; CODON; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE ASSOCIATION; ELECTRORETINOGRAM; GENE MUTATION; GENETIC ANALYSIS; GENETIC CONSERVATION; GENETIC TRAIT; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; LENS DISEASE; MOLECULAR EVOLUTION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FOLDING; SPECTRUM; VISUAL FIELD;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; CODON; CONSERVED SEQUENCE; EVOLUTION, MOLECULAR; GENE FREQUENCY; GENOTYPE; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; PHYLOGENY; RETINAL DISEASES; RETINITIS PIGMENTOSA; RHODOPSIN; SPECIES SPECIFICITY; VARIATION (GENETICS);

VERTEBRATA;

EID: 2442606621     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gene.2004.02.037     Document Type: Article

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