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Results 1 - 10 of 85 for Vitamin C
  1. African iron overload 
    ... leads to a faster-than-normal breakdown of vitamin C in the body, so affected individuals are at increased risk of vitamin C deficiency problems such as scurvy.People with African ...
    https://medlineplus.gov/genetics/condition/african-iron-overload - Genetics
  2. SLC2A10 gene 
    ... Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection. FEBS Lett. 2010 Jul 16;584(14): ...
    https://medlineplus.gov/genetics/gene/slc2a10 - Genetics
  3. Arterial tortuosity syndrome 
    ... Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection. FEBS Lett. 2010 Jul 16;584(14): ...
    https://medlineplus.gov/.../condition/arterial-tortuosity-syndrome - Genetics
  4. Tyrosinemia 
    ... are not genetic. The most likely causes are vitamin C deficiency or an immature liver due to premature ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
  5. MMACHC gene 
    ... Free article on PubMed Central Kim J, Gherasim C, Banerjee R. Decyanation of vitamin B12 by a trafficking chaperone. Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14551-4. doi: 10.1073/pnas.0805989105. Epub 2008 ... Tirone JC, Pawelek PD, Dore C, Atkinson JL, Watkins D, Morel CF, Fujiwara TM, ...
    https://medlineplus.gov/genetics/gene/mmachc - Genetics
  6. TTPA gene 
    ... on PubMed Meier R, Tomizaki T, Schulze-Briese C, Baumann U, Stocker A. The molecular basis of vitamin E retention: structure of human alpha-tocopherol transfer ...
    https://medlineplus.gov/genetics/gene/ttpa - Genetics
  7. VKORC1 gene 
    ... complex, subunit 1 VKOR Tests of VKORC1 PubMed VITAMIN K EPOXIDE REDUCTASE COMPLEX, SUBUNIT 1; VKORC1 NCBI Gene ClinVar Ferder NS, Eby CS, Deych E, Harris JK, Ridker PM, Milligan PE, ...
    https://medlineplus.gov/genetics/gene/vkorc1 - Genetics
  8. Pyridoxine-dependent epilepsy 
    ... Disorders (NORD) ClinicalTrials.gov EPILEPSY, EARLY-ONSET, 4, VITAMIN B6-DEPENDENT; EPEO4 PubMed Bok LA, Struys E, Willemsen MA, Been JV, Jakobs C. Pyridoxine-dependent seizures in Dutch patients: diagnosis by ...
    https://medlineplus.gov/.../condition/pyridoxine-dependent-epilepsy - Genetics
  9. Methylmalonic acidemia with homocystinuria 
    ... of methylmalonyl-coA mutase and homocysteine:methyltetrahydrofolate methyltransferase Vitamin B12 metabolic ... Cobalamin C disease Genetic Testing Registry: Methylmalonic aciduria and homocystinuria ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  10. FGF23 gene 
    ... doi: 10.1038/81664. Citation on PubMed Bergwitz C, Juppner H. Regulation of phosphate homeostasis by PTH, vitamin D, and FGF23. Annu Rev Med. 2010;61: ...
    https://medlineplus.gov/genetics/gene/fgf23 - Genetics
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