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Volumn 51, Issue 10, 2010, Pages 5304-5313

Retinal disease in Rpe65-deficient mice: Comparison to human leber congenital amaurosis due to RPE65 mutations

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGE DISTRIBUTION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; B WAVE; CELL ACTIVATION; CELL FUNCTION; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; ELECTRORETINOGRAM; GENE; GENE MUTATION; HUMAN; HUMAN CELL; ILLUMINATION; LEBER CONGENITAL AMAUROSIS; LIGHT INTENSITY; MOUSE; NONHUMAN; OPTICAL COHERENCE TOMOGRAPHY; PHOTORECEPTOR CELL; PHOTOSTIMULATION; PHOTOTRANSDUCTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA BIPOLAR GANGLION CELL; RETINA DISEASE; RPE65 GENE; SCHOOL CHILD; TOPOGRAPHY; VISUAL IMPAIRMENT; WAVEFORM; AGING; ANIMAL; C57BL MOUSE; COMPARATIVE STUDY; DARK ADAPTATION; ELECTRORETINOGRAPHY; GENETICS; MIDDLE AGED; MUTATION; PATHOPHYSIOLOGY; PHYSIOLOGY; RETINA DEGENERATION; TIME; VISION;

EID: 77958121723     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.10-5559     Document Type: Article
Times cited : (24)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.