Central retinal findings in Bothnia dystrophy caused by RLBP1 sequence variation

Archives of Ophthalmology

Volumn 128, Issue 8, 2010, Pages 989-995

  Burstedt, Marie S I ^a   Golovleva, Irina ^a  

^a UMEÅ UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BOTHNIA DYSTROPHY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; GENE; HUMAN; MALE; MISSENSE MUTATION; OPTICAL COHERENCE TOMOGRAPHY; PERIMETRY; PRIORITY JOURNAL; RETINA DYSTROPHY; RLBP1 GENE; SCHOOL CHILD; SCOTOMA; VISUAL ACUITY; VISUAL FIELD DEFECT;

ADOLESCENT; ADULT; CARRIER PROTEINS; CHILD; FEMALE; GENES, RECESSIVE; HUMANS; MALE; MUTATION, MISSENSE; PERIMETRY; RETINA; RETINITIS PIGMENTOSA; TOMOGRAPHY, OPTICAL COHERENCE; VISION DISORDERS; VISUAL ACUITY; VISUAL FIELDS; YOUNG ADULT;

EID: 77955455613     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2010.167     Document Type: Article

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