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Volumn 42, Issue 11, 2001, Pages 2728-2736
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Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene
a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ADOLESCENT;
ADULT;
ARTICLE;
CLINICAL ARTICLE;
ELECTRORETINOGRAM;
GAP JUNCTION;
GENE MUTATION;
HUMAN;
NIGHT BLINDNESS;
PRIORITY JOURNAL;
RETINA BIPOLAR GANGLION CELL;
RETINA CONE;
RETINA ROD;
ADOLESCENT;
ADULT;
CHILD;
DNA MUTATIONAL ANALYSIS;
ELECTRORETINOGRAPHY;
FLICKER FUSION;
HUMANS;
LINKAGE (GENETICS);
MIDDLE AGED;
MUTATION;
NIGHT BLINDNESS;
PROTEOGLYCANS;
RODS (RETINA);
VISUAL PATHWAYS;
X CHROMOSOME;
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EID: 0034799576
PISSN: 01460404
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (34)
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References (59)
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