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Results 1 - 10 of 87 for Vitamin B
  1. Imerslund-Gräsbeck syndrome 
    ... IGS1 PubMed Grasbeck R. Imerslund-Grasbeck syndrome (selective vitamin B(12) malabsorption with proteinuria). Orphanet J Rare Dis. ... anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15;96( ...
    https://medlineplus.gov/.../condition/imerslund-grasbeck-syndrome - Genetics
  2. Hereditary folate malabsorption 
    ... with the body's ability to absorb certain B vitamins (called folates) from food. Folates are important for ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  3. Cerebral folate transport deficiency 
    ... that develops from a shortage (deficiency) of the B-vitamin folate (also called vitamin B9) in the brain. ...
    https://medlineplus.gov/.../cerebral-folate-transport-deficiency - Genetics
  4. Methylmalonic acidemia with homocystinuria 
    ... LMBRD1: the gene for the cblF defect of vitamin B(1)(2) metabolism. J Inherit Metab Dis. 2011 ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  5. MMADHC gene 
    ... and MMADHC, two human proteins participating in intracellular vitamin B(1)(2) metabolism. Mol Genet Metab. 2011 Feb; ... M, Coelho D, Suormala T, Burda P, Fowler B, Baumgartner MR. Molecular mechanisms leading ... Epub 2011 Dec 8. Citation on PubMed
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  6. LMBRD1 gene 
    ... LMBRD1: the gene for the cblF defect of vitamin B(1)(2) metabolism. J Inherit Metab Dis. 2011 ...
    https://medlineplus.gov/genetics/gene/lmbrd1 - Genetics
  7. MMAA gene 
    ... MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent ...
    https://medlineplus.gov/genetics/gene/mmaa - Genetics
  8. CUBN gene 
    ... anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15;96(2):405-9. Citation on PubMed Watkins D, Rosenblatt DS. Lessons in biology from patients with inborn errors of vitamin B12 metabolism. Biochimie. 2013 May;95(5):1019- ...
    https://medlineplus.gov/genetics/gene/cubn - Genetics
  9. APOB gene 
    ... fat-soluble vitamins such as vitamin E and vitamin A.Apolipoprotein B-100, which is produced in the liver, is ... changes lead to a reduction of functional apolipoprotein B. As a result, the ... fats and fat-soluble vitamins from the diet, leading to the signs and ...
    https://medlineplus.gov/genetics/gene/apob - Genetics
  10. Biotinidase deficiency 
    ... enzyme called biotinidase. This enzyme recycles biotin, a B vitamin found in foods such as liver, egg yolks, ... Epub 2010 Jan 11. Citation on PubMed Wolf B. The neurology of biotinidase deficiency. Mol ... Epub 2011 Jun 12. Citation on PubMed
    https://medlineplus.gov/genetics/condition/biotinidase-deficiency - Genetics
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