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![]() Date: 2015-03-23 21:11:42Homocysteine Trimethylglycine Cofactors Vitamin B12 Methionine Folic acid Cystathionine beta synthase Chemistry Homocystinuria Quaternary ammonium compounds | Source URL: www.pbs.gov.auDownload Document from Source WebsiteFile Size: 69,60 KBShare Document on Facebook |
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![]() | Homocystinuria What is homocystinuria? Homocystinuria is an inherited condition that affects the way a person’s body uses a part of food called methionine (a precursor to homocystine). A person with homocystinuria cannDocID: Haei - View Document |
![]() | Homocystinuria Homocystinuria is an autosomal recessive disorder of methionine metabolism. The most common cause of homocystinuria is a deficiency of the amino acid cystathionine B-synthase. Due to this deficiency, elevaDocID: DKpB - View Document |