Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene

Archives of Ophthalmology

Volumn 128, Issue 6, 2010, Pages 772-778

  Hugosson, Therése ^a,c   Friedman, James S ^d   Ponjavic, Vesna ^a   Abrahamson, Magnus ^b   Swaroop, Anand ^d,e   Andréasson, Sten ^a  

^a LUND UNIVERSITY   (Sweden)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

^c CENTRAL HOSPITAL   (Sweden)

^d NATIONAL EYE INSTITUTE   (United States)

^e UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; ELECTROPHYSIOLOGY; ELECTRORETINOGRAPHY; EXON; EYE FUNDUS; FOLLOW UP; GENE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; KLHL7 GENE; OPHTHALMOLOGY; OPTICAL COHERENCE TOMOGRAPHY; PERIMETRY; PHENOTYPE; PRIORITY JOURNAL; RETINA CONE; RETINA DEGENERATION; RETINA ROD; RETINITIS PIGMENTOSA; SEQUENCE ANALYSIS; VISUAL ACUITY;

ADOLESCENT; ADULT; AGED; AUTOANTIGENS; ELECTRORETINOGRAPHY; FEMALE; GENES, DOMINANT; HUMANS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PERIMETRY; PHENOTYPE; REGISTRIES; RETINITIS PIGMENTOSA; SWEDEN; TOMOGRAPHY, OPTICAL COHERENCE; VISUAL ACUITY; VISUAL FIELDS; YOUNG ADULT;

EID: 77953627257     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2010.98     Document Type: Article

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