Medicine & Life Sciences
Gyrate Atrophy
100%
Ornithine-Oxo-Acid Transaminase
84%
Genes
64%
Ornithine
58%
Peroxisomes
44%
Proline
43%
Mutation
42%
delta-1-pyrroline-5-carboxylate
41%
Peroxisome biogenesis disorders
31%
Phenotype
28%
Arginine
26%
Proline Oxidase
26%
Complementary DNA
23%
Alleles
23%
human OAT protein
22%
Proteins
21%
Schizophrenia
21%
Genomics
20%
Obsessive-Compulsive Disorder
19%
Enzymes
19%
Fibroblasts
17%
Exons
17%
Hyperammonemia
17%
Retinal Degeneration
16%
Hyperprolinemia type 2
16%
Rhizomelic Chondrodysplasia Punctata
15%
Single Nucleotide Polymorphism
15%
Diet
15%
ATP-Binding Cassette Transporters
14%
Amino Acids
13%
ATP Binding Cassette Transporter, Subfamily D, Member 1
13%
Organism Cloning
13%
Pyrroline Carboxylate Reductases
13%
Exome
13%
Membrane Proteins
12%
3-methylcrotonyl CoA carboxylase 1 deficiency
12%
Genetic Association Studies
11%
Inborn Genetic Diseases
11%
1-Pyrroline-5-Carboxylate Dehydrogenase
11%
Peroxisome-Targeting Signal 1 Receptor
11%
Genome
11%
Peroxisomal Targeting Signal 2 Receptor
11%
Intellectual Disability
11%
Genetic Databases
10%
Ornithine Carbamoyltransferase Deficiency Disease
10%
Retina
9%
Pyridoxine
9%
Saccharomyces cerevisiae
9%
Yeasts
9%