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Annals of Medicine, ISSN 0785-3890, 12/2013, Volume 45, Issue 8, pp. 522 - 531
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2009, Volume 41, Issue 2, pp. 234 - 239
Vitamin B(12) (cobalamin) is essential in animals for metabolism of branched chain amino acids and odd chain fatty acids, and for remethylation of homocysteine... 
Vitamin B 12 Deficiency - etiology | Transcobalamins - genetics | Humans | Male | Methylmalonic Acid - metabolism | Proteins - isolation & purification | Tissue Distribution | Membrane Transport Proteins - deficiency | Membrane Transport Proteins - genetics | Transcobalamins - isolation & purification | Female | Membrane Transport Proteins - metabolism | Vitamin B 12 Deficiency - metabolism | Child | Methylmalonic Acid - urine | Chromosome Deletion | Lysosome-Associated Membrane Glycoproteins - metabolism | Nucleocytoplasmic Transport Proteins - physiology | Chromosome Mapping | Chromosomes, Human, Pair 6 | Nucleocytoplasmic Transport Proteins - genetics | Polymorphism, Genetic | Proteins - genetics | Nucleocytoplasmic Transport Proteins - metabolism | Proteins - metabolism | Transcobalamins - metabolism | Vitamin B 12 Deficiency - genetics | Hyperhomocysteinemia - genetics | HeLa Cells | Hyperhomocysteinemia - complications | Vitamin B 12 - metabolism | Medical research | Heart surgery | Genes | Vitamin B | Genetics | Medical screening | Chromosomes | Nucleocytoplasmic Transport Proteins | Biochemistry, Molecular Biology | Vitamin B 12 Deficiency | Proteins | Life Sciences | Membrane Transport Proteins | Transcobalamins | Vitamin B 12 | Hyperhomocysteinemia | Methylmalonic Acid | Lysosome-Associated Membrane Glycoproteins | Hela Cells
Journal Article
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 02/2011, Volume 157, Issue 1, pp. 33 - 44
Derivatives of cobalamin (vitamin B12) are required for activity of two enzymes in humans. Adenosylcobalamin is required for activity of mitochondrial... 
methylmalonic acidemia | vitamin B12 | cobalamin | homocystinuria | transcobalamin | Methylmalonic acidemia | Cobalamin | Transcobalamin | Homocystinuria | Vitamin B12 | VITAMIN-B12 METABOLISM | COMPLEMENTATION GROUP | COMBINED METHYLMALONIC ACIDURIA | METHIONINE SYNTHASE REDUCTASE | METHYLCOBALAMIN DEFICIENCY | GENETICS & HEREDITY | TRANSCOBALAMIN-I HAPTOCORRIN | MEGALOBLASTIC-ANEMIA | GENETIC COMPLEMENTATION | MOUSE GASTRULATION | INTRINSIC-FACTOR | Malabsorption Syndromes - diagnosis | Methylmalonic Acid - blood | Humans | Vitamin B 12 - analogs & derivatives | Hyperhomocysteinemia - metabolism | Malabsorption Syndromes - metabolism | Neonatal Screening | Amino Acid Metabolism, Inborn Errors - diagnosis | Methylmalonyl-CoA Mutase - metabolism | Amino Acid Metabolism, Inborn Errors - metabolism | Homocysteine - urine | Anemia, Megaloblastic | Proteinuria - diagnosis | Vitamin B 12 Deficiency - metabolism | Infant, Newborn | Methylmalonic Acid - urine | Cobamides - metabolism | Vitamin B 12 Deficiency - diagnosis | Metabolism, Inborn Errors - metabolism | Homocysteine - blood | Proteinuria - metabolism | Methylmalonyl-CoA Mutase - deficiency | Metabolism, Inborn Errors - diagnosis | Vitamin B 12 Deficiency - genetics | Hyperhomocysteinemia - diagnosis | Vitamin B 12 - metabolism | Thrombocytopenia | Urine | homocysteine | Enzymes | 5-Methyltetrahydrofolate-homocysteine S-methyltransferase | Anemia | adenosylcobalamin | Blood | Psychosis | Mitochondria | Dementia disorders | Complementation | Degeneration | Metabolic acidosis | Neutropenia
Journal Article
AMERICAN JOURNAL OF PATHOLOGY, ISSN 0002-9440, 01/2018, Volume 188, Issue 1, pp. 160 - 172
Journal Article
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 05/2017, Volume 114, Issue 20, pp. E4095 - E4102
Journal Article