1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17389517&form=6&db=m	The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.	causal interaction,diagnostic usage,therapeutic application,unassigned	4,3,1,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17512723&form=6&db=m	RDH12, a retinol dehydrogenase causing Leber's congenital amaurosis, is also involved in steroid metabolism.	causal interaction,unassigned	3,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17512964&form=6&db=m	Novel RDH12 mutations associated with Leber congenital amaurosis and cone-rod dystrophy: biochemical and clinical evaluations.	causal interaction,ongoing research,unassigned	3,2,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18326732&form=6&db=m	Retinol dehydrogenases RDH11 and RDH12 in the mouse retina: expression levels during development and regulation by oxidative stress.	causal interaction,unassigned	3,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19686838&form=6&db=m	Retinol dehydrogenase 12 detoxifies 4-hydroxynonenal in photoreceptor cells.	therapeutic application,unassigned	1,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19840725&form=6&db=m	Which Leber congenital amaurosis patients are eligible for gene therapy trials?	causal interaction,diagnostic usage,unassigned	1,1,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20736127&form=6&db=m	Novel RDH12 sequence variations in Leber congenital amaurosis.	unassigned	-	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22621924&form=6&db=m	Reduction of all-trans-retinal in vertebrate rod photoreceptors requires the combined action of RDH8 and RDH12.	causal interaction,unassigned	3,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25148430&form=6&db=m	Genome-wide homozygosity mapping in families with leber congenital amaurosis identifies mutations in AIPL1 and RDH12 genes.	diagnostic usage,unassigned	3,0	
1.1.1.105	Blindness	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27809489&form=6&db=m	Structural Insights into the Drosophila melanogaster Retinol Dehydrogenase, a Member of the Short-Chain Dehydrogenase/Reductase Family.	ongoing research,unassigned	2,0