ISSN: 2153-0637
Glycine encephalopathy is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism. The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism.
Review Article: Journal of Glycomics & Lipidomics
Research Article: Journal of Glycomics & Lipidomics
Review Article: Journal of Glycomics & Lipidomics
Review Article: Journal of Glycomics & Lipidomics
Research Article: Journal of Glycomics & Lipidomics
Scientific Tracks Abstracts: Journal of Proteomics & Bioinformatics
Posters & Accepted Abstracts: Journal of Proteomics & Bioinformatics
Scientific Tracks Abstracts: Journal of Proteomics & Bioinformatics
Posters-Accepted Abstracts: Journal of Proteomics & Bioinformatics