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Results 11 - 20 of 44 for vitamin C
  1. MMADHC gene 
    ... J, Paquette SG, Gagnon H, Ng-Thow-Hing C, Gibbs BF, Hancock MA, Rosenblatt DS, Coulton JW. Interaction between MMACHC and MMADHC, two human proteins participating in intracellular vitamin B(1)(2) metabolism. Mol Genet Metab. 2011 ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  2. AMN gene 
    ... 23. Citation on PubMed Kozyraki R, Cases O. Vitamin B12 ... Namour F, Dobrovoljski G, Chery C, Audonnet S, Feillet F, Sperl W, Gueant JL. ...
    https://medlineplus.gov/genetics/gene/amn - Genetics
  3. CYP24A1 gene 
    ... a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D ... M, Weber S, Irwin A, Goos C, John U, Misselwitz J, Klaus G, Kuwertz-Broking ...
    https://medlineplus.gov/genetics/gene/cyp24a1 - Genetics
  4. HCFC1 gene 
    ... X-linked disability, but does not severely impact vitamin B12 processing. CFF HCF HCF-1 HCF1 ... Gerard M, Morin G, Bourillon A, Colson C, Mathieu S, Rabier D, Billette de Villemeur T, ...
    https://medlineplus.gov/genetics/gene/hcfc1 - Genetics
  5. HSD3B7 gene 
    ... build up in the liver and fat-soluble vitamins are not absorbed, leading to the signs and symptoms of ... steroid oxidoreductase 3BHS7_HUMAN c(27) 3-beta-HSD C(27)-3BETA-HSD ...
    https://medlineplus.gov/genetics/gene/hsd3b7 - Genetics
  6. PRDX1 gene 
    ... M, Watkins D, Pastinen T, Chung WK, Ficicioglu C, Feillet F, Froese DS, Baumgartner ... metabolism of vitamin B12. Clin Epigenetics. 2022 Apr 19;14(1): ...
    https://medlineplus.gov/genetics/gene/prdx1 - Genetics
  7. SAR1B gene 
    ... absorption (malabsorption) of dietary fats and fat-soluble vitamins, leading to nutritional and developmental problems in people with ... Charcosset M, Sassolas A, Peretti N, Roy CC, Deslandres C, Sinnett D, Levy E, Lachaux A. Anderson or ...
    https://medlineplus.gov/genetics/gene/sar1b - Genetics
  8. SLC34A1 gene 
    ... Kaneko I, Tatsumi S, Segawa H, Miyamoto K. Vitamin D and type II sodium-dependent ... C, Grandchamp B, Friedlander G. Nephrolithiasis and osteoporosis associated ...
    https://medlineplus.gov/genetics/gene/slc34a1 - Genetics
  9. SLC6A19 gene 
    ... these features are related to a deficiency of vitamin B3 (niacin) and one of its main components, the amino acid tryptophan. More ... Azmanov DN, Rodgers H, Auray-Blais C, Giguere R, Bailey C, Broer S, Rasko JE, ...
    https://medlineplus.gov/genetics/gene/slc6a19 - Genetics
  10. ALDH7A1 gene 
    ... in the activity of pyridoxine, a form of vitamin B6 derived from food. Pyridoxine plays a role many processes in the body, such as ... Bok LA, Struys E, Willemsen MA, Been JV, Jakobs C. Pyridoxine-dependent seizures in Dutch patients: diagnosis by ...
    https://medlineplus.gov/genetics/gene/aldh7a1 - Genetics
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