GCAP1 mutations associated with autosomal dominant cone dystrophy

Advances in Experimental Medicine and Biology

Volumn 664, Issue , 2010, Pages 273-282

  Jiang, Li ^b   Baehr, Wolfgang ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; GUANYLATE CYCLASE; GUANYLATE CYCLASE ACTIVATING PROTEIN 1; GUANYLATE CYCLASE ACTIVATOR; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT CONE DYSTROPHY; BINDING AFFINITY; CALCIUM BINDING; CALCIUM CELL LEVEL; CONFERENCE PAPER; GAIN OF FUNCTION MUTATION; GENE MUTATION; GUCA1A GENE; HUMAN; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; RETINA DYSTROPHY; RETINA ROD;

AMINO ACID SEQUENCE; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; GUANYLATE CYCLASE; GUANYLATE CYCLASE-ACTIVATING PROTEINS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; RETINITIS PIGMENTOSA;

EID: 79959594780     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4419-1399-9_31     Document Type: Conference Paper

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