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NYX gene

Known as: CLRP, NYCTALOPIN, CSNB1A 
National Institutes of Health

Papers overview

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2015
2015
Purpose Mutations in the NYX gene are known to cause complete congenital stationary night blindness (CSNB1), which is always… 
2013
2013
PURPOSE Complete congenital stationary night blindness (CSNB1) is characterized by loss of night vision due to a defect in the… 
2012
2012
Nyctalopin is a small leucine rich repeat proteoglycan (SLRP) whose function is critical for normal vision. The absence of… 
2006
2006
AbstractX-linked congenital stationary night blindness (CSNB) and NYX mutation have not been reported in Chinese. Here, two… 
2005
2005
Mutations in the gene NYX, which encodes nyctalopin, lead to the retinal disorder congenital stationary night blindness which is… 
2003
2003
PURPOSE The complete type of X-linked congenital stationary night blindness (CSNB1) in human and mouse is caused by mutations in… 
2003
2003
PURPOSE It has been shown recently that mutations in NYX (nyctalopin on chromosome X), encoding a novel protein associated with… 
1992
1992
Anaerobic production of extracellular polysaccharide (EP) was examined, using a previously uncharacterized, obligately anaerobic…