Characterizing the phenotype and genotype of a family with occult macular dystrophy

Archives of Ophthalmology

Volumn 130, Issue 12, 2012, Pages 1554-1559

  Scholl, Hendrik P N ^a   Birch, David G ^c   Iwata, Takeshi ^b   Miller, Neil R ^a   Goldberg, Morton F ^a   Chen, Connie J ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

^b National Hospital Organization   (Japan)

^c UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN; RETINITIS PIGMENTOSA 1 LIKE 1 PROTEIN; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; AUTOFLUORESCENCE; CLINICAL ARTICLE; COLOR VISION TEST; CROSS-SECTIONAL STUDY; ELECTRORETINOGRAPHY; EYE PHOTOGRAPHY; FAMILY; FEMALE; GENETIC SCREENING; GENOTYPE; HUMAN; JAPANESE; MALE; MUTATIONAL ANALYSIS; OBSERVATIONAL STUDY; OCCULT MACULAR DYSTROPHY; OPHTHALMOSCOPY; PERIMETRY; PHENOTYPE; PHOTORECEPTOR INNER SEGMENT; PHOTORECEPTOR OUTER SEGMENT; PRIORITY JOURNAL; RETINA FLUORESCEIN ANGIOGRAPHY; RETINA MACULA DEGENERATION; SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY;

ADULT; CROSS-SECTIONAL STUDIES; ELECTRORETINOGRAPHY; EUROPEAN CONTINENTAL ANCESTRY GROUP; EYE PROTEINS; FEMALE; GENOTYPE; HUMANS; MACULA LUTEA; MACULAR DEGENERATION; MALE; PHENOTYPE; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 84871254093     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2012.2683     Document Type: Article

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