Medicine & Life Sciences
Hypermethioninemia
100%
Mutation
92%
Epilepsy
86%
Genes
82%
Lactic Acidosis
77%
carglumic acid
72%
Inborn Urea Cycle Disorder
66%
Hyperammonemia
65%
Intellectual Disability
65%
Oxidoreductases
63%
Glutamate Synthase
62%
Hyperargininemia
61%
Exome
60%
Homocysteinemia
56%
Pediatrics
56%
Methionine
54%
Methylmalonic acidemia
53%
Atypical Hemolytic Uremic Syndrome
52%
Hereditary Spastic Paraplegia
51%
Achondroplasia
51%
DNA Polymerase beta
51%
Heterozygote
49%
Metabolomics
47%
Inborn Errors Metabolism
44%
Chromosomes, Human, Pair 7
44%
Mitochondrial Diseases
43%
Homocysteine
43%
2-Hydroxyglutaricaciduria
41%
Proteins
40%
Methylmalonic Acid
39%
Germ-Line Mutation
39%
DNA-Binding Proteins
38%
Vitamin B 12
38%
Homozygote
38%
Scoliosis
37%
Mucins
37%
Mitochondrial DNA
36%
Microarray Analysis
35%
Thrombotic Microangiopathies
35%
Genomics
35%
Postpartum Period
33%
Lipoylation
32%
Histones
32%
Milk
32%
Adenosine Triphosphate
32%
Child
31%
Organism Cloning
31%
Chromatin
30%
Glutamic Acid
30%
Neurodegenerative Diseases
30%
Chemical Compounds
Core Protein
45%
Disorder
42%
Carglumic Acid
40%
Complementary DNA
36%
Mutation
35%
Nucleotide
28%
Metabolic
27%
Pharmacological Metabolism
26%
Methionine
23%
Developmental
18%
Serum Level
15%
Error
15%
Glutamine
15%
Homocysteine
14%
Protein
14%
Urea
13%
Carbamoyl Phosphate
13%
2-Hydroxyglutarate
12%
Electron Transport
8%
Peptide
8%
Dimerization
7%
Acid
6%
Glycoprotein
6%
Isotope
5%