Title : NMNAT1 mutations cause Leber congenital amaurosis.

Pub. Date : 2012 Sep

PMID : 22842227






4 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 NMNAT1 resides in the previously identified LCA9 locus and encodes the nuclear isoform of nicotinamide mononucleotide adenylyltransferase, a rate-limiting enzyme in nicotinamide adenine dinucleotide (NAD(+)) biosynthesis(4,5). NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
2 NMNAT1 resides in the previously identified LCA9 locus and encodes the nuclear isoform of nicotinamide mononucleotide adenylyltransferase, a rate-limiting enzyme in nicotinamide adenine dinucleotide (NAD(+)) biosynthesis(4,5). NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
3 NMNAT1 resides in the previously identified LCA9 locus and encodes the nuclear isoform of nicotinamide mononucleotide adenylyltransferase, a rate-limiting enzyme in nicotinamide adenine dinucleotide (NAD(+)) biosynthesis(4,5). NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
4 NMNAT1 resides in the previously identified LCA9 locus and encodes the nuclear isoform of nicotinamide mononucleotide adenylyltransferase, a rate-limiting enzyme in nicotinamide adenine dinucleotide (NAD(+)) biosynthesis(4,5). NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens