Gene: NXNL1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115861
Gene Symbol: NXNL1
NXNL1 		0.010 Biomarker group BEFREE Because the secondary loss of cones in retinitis pigmentosa (RP) leads to blindness, the administration of RdCVF is a promising therapy for this untreatable neurodegenerative disease. 25957687 2015