Detailed analysis of retinal function and morphology in a patient with autosomal recessive bestrophinopathy (ARB)

Documenta Ophthalmologica

Volumn 118, Issue 3, 2009, Pages 239-246

  Gerth, Christina ^a,b   Zawadzki, Robert J ^c   Werner, John S ^c   Héon, Elise ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF ROSTOCK   (Germany)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

ARB; Autosomal recessive bestrophinopathy; Electro oculogram; Fourier domain OCT; Multifocal ERG

Indexed keywords

BESTROPHIN 1; MEMBRANE PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE BESTROPHINOPATHY; CASE REPORT; CHILD; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; GENE MUTATION; HETEROZYGOSITY; HUMAN; MALE; OPTICAL COHERENCE TOMOGRAPHY; PHOTORECEPTOR; PIGMENT EPITHELIUM; RETINA DETACHMENT; RETINA DYSTROPHY; SCHOOL CHILD; VISUAL ACUITY;

ALLELES; CHILD; CHLORIDE CHANNELS; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; EYE PROTEINS; FOURIER ANALYSIS; FUNDUS OCULI; GENES, RECESSIVE; HUMANS; MALE; MUTATION; PHOTORECEPTOR CELLS, VERTEBRATE; RETINA; RETINAL DISEASES; RETINAL PIGMENT EPITHELIUM; TOMOGRAPHY, OPTICAL COHERENCE; VISION, OCULAR;

EID: 67349108326     PISSN: 00124486     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10633-008-9154-5     Document Type: Article

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