Galactosemia is a potentially fatal disease resulting from a deficiency of galactose-1-phosphate uridyl transferase. In order to perform mechanistic studies designed to elucidate further the etiology of the disease, we required a method to monitor 13 C enrichment in plasma galactose following a sing
✦ LIBER ✦
Determination of (-)-threo-chlorocitric acid in human plasma by gas chromatography—positive chemical-ionization mass spectrometry
✍ Scribed by F. Rubio; F. de Grazia; B.J. Miwa; W.A. Garland
- Book ID
- 108448165
- Publisher
- Elsevier Science
- Year
- 1982
- Weight
- 483 KB
- Volume
- 233
- Category
- Article
- ISSN
- 0378-4347
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