Phenotypes in defined genotypes including siblings with usher syndrome

Ophthalmic Genetics

Volumn 32, Issue 2, 2011, Pages 65-74

  Malm, Eva ^a   Ponjavic, Vesna ^a   Möller, Claes ^b   Kimberling, William J ^c,d   Andréasson, Sten ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b ÖREBRO UNIVERSITY HOSPITAL   (Sweden)

^c UNIVERSITY OF IOWA   (United States)

^d BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

Electroretinography; Optical coherence tomography; Usher syndrome

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; ELECTRORETINOGRAPHY; FEMALE; GENETIC ANALYSIS; GENOTYPE; HUMAN; MALE; OPTICAL COHERENCE TOMOGRAPHY; PERIMETRY; PRIORITY JOURNAL; RETINA FOVEA; USHER SYNDROME; VISION;

ADOLESCENT; ADULT; AGED; CADHERINS; CHILD; ELECTRORETINOGRAPHY; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENOTYPE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MYOSINS; PEDIGREE; PHENOTYPE; QUESTIONNAIRES; RECEPTORS, G-PROTEIN-COUPLED; RETINA; SIBLINGS; TOMOGRAPHY, OPTICAL COHERENCE; USHER SYNDROMES; VISUAL ACUITY; VISUAL FIELDS;

EID: 79955809485     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.3109/13816810.2010.536064     Document Type: Article

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