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NATURE GENETICS, ISSN 1061-4036, 07/1998, Volume 19, Issue 3, pp. 264 - 267
X-linked congenital stationary night blindness (CSNB) is a recessive non-progressive retinal disorder characterized by night blindness, decreased visual... 
SUBTYPE | B-WAVE | DNA | GENETICS & HEREDITY | ELECTRORETINOGRAM | EXPRESSION
Journal Article
Nature genetics, ISSN 1061-4036, 2000, Volume 26, Issue 3, pp. 319 - 323
Journal Article
Journal of Cardiac Failure, ISSN 1071-9164, 2012, Volume 18, Issue 6, pp. 446 - 458
Journal Article
Journal of Immunology, ISSN 0022-1767, 08/1996, Volume 157, Issue 4, pp. 1474 - 1484
To investigate the molecular events associated with B cell apoptosis, we analyzed follicular B cells from the large Peyer's patch (PP) in the sheep ileum. Over... 
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2000, Volume 26, Issue 3, pp. 319 - 323
During development, visual photoreceptors, bipolar cells and other neurons establish connections within the retina enabling the eye to process visual images... 
nyctalopin | NYX gene
Journal Article
Nature genetics, ISSN 1061-4036, 07/1998, Volume 19, Issue 3, p. 264
X-linked congenital stationary night blindness (CSNB) is a recessive non-progressive retinal disorder characterized by night blindness, decreased visual... 
Amino Acid Sequence | Exons | Humans | Molecular Sequence Data | Calcium Channels, L-Type | Male | Night Blindness - congenital | Tissue Distribution | Calcium Channels - physiology | Pedigree | Base Sequence | X Chromosome | Female | Mutation | Calcium Channels - genetics | Night Blindness - genetics | DNA, Complementary
Journal Article
Nature Genetics, ISSN 1061-4036, 07/1998, Volume 19, Issue 3, pp. 264 - 267
X-linked congenital stationary night blindness (CSNB) is a recessive non-progressive retinal disorder characterized by night blindness, decreased visual... 
Journal Article
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