Macular dysfunction in Oguchi disease with the frequent mutation 1147delA in the SAG gene

Ophthalmic Research

Volumn 46, Issue 4, 2011, Pages 175-180

  Hayashi, Takaaki ^a   Tsuzuranuki, Satoshi ^a   Kozaki, Kenichi ^a   Urashima, Mitsuyoshi ^a   Tsuneoka, Hiroshi ^a  

^a JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Full field electroretinography; Multifocal electroretinography; Mutation; Optical coherence tomography; SAG gene

Indexed keywords

RETINA S ANTIGEN; GRK1 PROTEIN, HUMAN; RHODOPSIN KINASE;

ADULT; ARTICLE; CASE REPORT; ELECTRORETINOGRAM; EYE EXAMINATION; FULL FIELD ELECTRORETINOGRAM; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMPHREY VISUAL FIELD TESTING; MALE; MULTIFOCAL ELECTRORETINOGRAM; OGUCHI DISEASE; OPHTHALMOSCOPY; OPTICAL COHERENCE TOMOGRAPHY; OUTER NUCLEAR LAYER; PHOTORECEPTOR INNER SEGMENT; PRIORITY JOURNAL; RETINA; RETINA DISEASE; RETINA MACULOPATHY; RETINA ROD; RETINAL PIGMENT EPITHELIUM ATROPHY; VISION TEST; ELECTRORETINOGRAPHY; GENETICS; NIGHT BLINDNESS; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PERIMETRY; PHYSIOLOGY; POLYMERASE CHAIN REACTION; RETINAL DISEASES; VISION DISORDERS; VISUAL FIELD;

ADULT; ARRESTIN; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; G-PROTEIN-COUPLED RECEPTOR KINASE 1; HUMANS; MALE; NIGHT BLINDNESS; POLYMERASE CHAIN REACTION; RETINA; RETINAL DISEASES; SEQUENCE DELETION; TOMOGRAPHY, OPTICAL COHERENCE; VISION DISORDERS; VISUAL FIELD TESTS; VISUAL FIELDS;

EID: 79953059275     PISSN: 00303747     EISSN: 14230259     Source Type: Journal    
DOI: 10.1159/000325024     Document Type: Article

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