Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets

Eye

Volumn 23, Issue 1, 2009, Pages 230-233

  Aleman, T S ^a   Lam, B L ^b   Cideciyan, A V ^a   Sumaroka, A ^a   Windsor, E A M ^a   Roman, A J ^a   Schwartz, S B ^a   Stone, E M ^c   Jacobson, S G ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF IOWA   (United States)

Author keywords

Electroretinogram; Optical coherence tomography; Retinal circuitry; Retinitis pigmentosa

Indexed keywords

ADULT; ANAMNESIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; DNA SEQUENCE; ELECTRORETINOGRAM; FEMALE; GENE; GENETIC HETEROGENEITY; HETEROZYGOSITY; HUMAN; OPTICAL COHERENCE TOMOGRAPHY; PEDIGREE ANALYSIS; PERIMETRY; PHENOTYPE; PRPF31 GENE; RETINA CONE; RETINA ROD; RETINITIS PIGMENTOSA; VISUAL ACUITY;

EID: 58249106836     PISSN: 0950222X     EISSN: 14765454     Source Type: Journal    
DOI: 10.1038/eye.2008.264     Document Type: Article

References (5)

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