Viktor Kožich Henk Blom Stefan Kölker Marike Groenendijk Outline

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Date: 2014-12-08 11:13:53 Homocysteine Coenzymes Methylenetetrahydrofolate reductase Cystathionine beta synthase Methionine S-Adenosyl methionine S-Adenosyl-L-homocysteine Chemistry Homocystinuria Vitamin B12		Viktor Kožich Henk Blom Stefan Kölker Marike Groenendijk Outline Add to Reading List Source URL: ec.europa.eu Download Document from Source Website File Size: 1,75 MB Share 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 cann DocID: 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, eleva DocID: DKpB - View Document