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|Title:||Plasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infant|
Chulabhorn Research Institute
|Citation:||Southeast Asian Journal of Tropical Medicine and Public Health. Vol.30, No.SUPPL. 2 (1999), 140-142|
|Abstract:||Methylmalonic acidemia is an inborn error of organic acid metabolism resulting from defects in methylmalonyl CoA mutase. Analysis of plasma free amino acids in a 15-month-old Thai infant by HPLC showed marked elevation of glycine. HPLC analysis of urinary organic acids showed high levels of methylmalonic acid.|
|Appears in Collections:||Scopus 1991-2000|
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