Pub. Date : 2015 Jul 10
PMID : 26018082
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Leber congenital amaurosis 9 (LCA9) is an autosomal recessive retinal degeneration condition caused by mutations in the NAD(+) biosynthetic enzyme NMNAT1. | NAD | nicotinamide nucleotide adenylyltransferase 1 | Homo sapiens |