<--- Back to Details
First PageDocument Content
Homocysteine / Trimethylglycine / Cofactors / Vitamin B12 / Methionine / Folic acid / Cystathionine beta synthase / Chemistry / Homocystinuria / Quaternary ammonium compounds
Date: 2015-03-23 21:11:42
Homocysteine
Trimethylglycine
Cofactors
Vitamin B12
Methionine
Folic acid
Cystathionine beta synthase
Chemistry
Homocystinuria
Quaternary ammonium compounds

Add to Reading List

Source URL: www.pbs.gov.au

Download Document from Source Website

File Size: 69,60 KB

Share Document on Facebook

Similar Documents

Homocysteine / Trimethylglycine / Cofactors / Vitamin B12 / Methionine / Folic acid / Cystathionine beta synthase / Chemistry / Homocystinuria / Quaternary ammonium compounds

PDF Document

DocID: 17lG6 - View Document

Proteinogenic amino acids / Vitamin B12 / Cofactors / Methionine / Glutathione / S-Adenosyl methionine / Homocysteine / Cysteine / Cystathionine beta synthase / Chemistry / Thiols / Glucogenic amino acids

Microsoft PowerPoint - 3 dick Deth Methylation Panel.ppt

DocID: S39y - View Document

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

DocID: PDjV - View Document

Homocystinuria / Rare diseases / Cystathionine beta synthase / Homocysteine / Recessive / Methionine / Cystinuria / Phenylketonuria / Newborn screening / Medicine / Health / Genetic genealogy

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 / Homocysteine / Marfan syndrome / Methionine / Cystathionine beta synthase / Cystinuria / Newborn screening / Hypermethioninemia / Health / Chemistry / Genetic genealogy

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