Retinal morphology in patients with BBS1 and BBS10 related Bardet-Biedl Syndrome evaluated by Fourier-domain optical coherence tomography

Vision Research

Volumn 48, Issue 3, 2008, Pages 392-399

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

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Bardet Biedl Syndrome; BBS1; BBS10; Fourier domain OCT; Retinal lamination

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BARDET BIEDL SYNDROME; BBS1 GENE; BBS10 GENE; BRUCH MEMBRANE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE; GENE MUTATION; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; IMAGE ANALYSIS; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; OPTICAL COHERENCE TOMOGRAPHY; PRIORITY JOURNAL; RETINA DYSTROPHY; RETINA IMAGE; SCHOOL CHILD;

ADOLESCENT; ADULT; BARDET-BIEDL SYNDROME; CHAPERONINS; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; MALE; MUTATION; PHENOTYPE; PROTEINS; RETINA; RETINITIS PIGMENTOSA; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 38749122052     PISSN: 00426989     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.visres.2007.08.024     Document Type: Article

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