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Volumn 121, Issue 1, 2014, Pages 234-245

Retinal structure and function in achromatopsia: Implications for gene therapy

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CNGA3 GENE; CNGB3 GENE; COLOR BLINDNESS; CROSS-SECTIONAL STUDY; EXON; FEMALE; GENE; GENE THERAPY; GENETIC SCREENING; GENOTYPE; GNAT2 GENE; HUMAN; MALE; PDE6C GENE; PHOTORECEPTOR; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA; RETINA GYRATE ATROPHY; RETINAL THICKNESS; SCHOOL CHILD; SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY; YOUNG ADULT;

EID: 84891626222     PISSN: 01616420     EISSN: 15494713     Source Type: Journal    
DOI: 10.1016/j.ophtha.2013.08.017     Document Type: Article
Times cited : (144)

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