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Volumn 54, Issue 13, 2013, Pages 8181-8190
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A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations.
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Author keywords
[No Author keywords available]
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Indexed keywords
ABC TRANSPORTER;
ABCA4 PROTEIN, HUMAN;
DNA;
ADOLESCENT;
ADULT;
AGED;
CHILD;
COMPARATIVE STUDY;
DISEASE COURSE;
ELECTRORETINOGRAPHY;
EYE FUNDUS;
FEMALE;
FLUORESCENCE ANGIOGRAPHY;
FOLLOW UP;
GENETICS;
GENOTYPE;
HUMAN;
MACULAR DEGENERATION;
MALE;
METABOLISM;
MIDDLE AGED;
MUTATION;
NUCLEOTIDE SEQUENCE;
OPHTHALMOSCOPY;
PATHOLOGY;
PIGMENT EPITHELIUM;
PRESCHOOL CHILD;
PROCEDURES;
YOUNG ADULT;
ADOLESCENT;
ADULT;
AGED;
ATP-BINDING CASSETTE TRANSPORTERS;
CHILD;
CHILD, PRESCHOOL;
DISEASE PROGRESSION;
DNA;
DNA MUTATIONAL ANALYSIS;
ELECTRORETINOGRAPHY;
FEMALE;
FLUORESCEIN ANGIOGRAPHY;
FOLLOW-UP STUDIES;
FUNDUS OCULI;
GENOTYPE;
HUMANS;
MACULAR DEGENERATION;
MALE;
MIDDLE AGED;
MUTATION;
OPHTHALMOSCOPY;
RETINAL PIGMENT EPITHELIUM;
YOUNG ADULT;
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EID: 84894541201
PISSN: None
EISSN: 15525783
Source Type: Journal
DOI: 10.1167/iovs.13-12104 Document Type: Article |
Times cited : (122)
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References (0)
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