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Plasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infant

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dc.contributor.authorChantragan Srisomsapen_US
dc.contributor.authorPornswan Wasanten_US
dc.contributor.authorJisnuson Svastien_US
dc.contributor.authorDaranee Chokchaichamnankiten_US
dc.contributor.authorSomporn Liammongkolkulen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-07T08:53:59Z
dc.date.available2018-09-07T08:53:59Z
dc.date.issued1999-12-01en_US
dc.description.abstractMethylmalonic 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.en_US
dc.identifier.citationSoutheast Asian Journal of Tropical Medicine and Public Health. Vol.30, No.SUPPL. 2 (1999), 140-142en_US
dc.identifier.issn01251562en_US
dc.identifier.other2-s2.0-0347811687en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/25539
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0347811687&origin=inwarden_US
dc.subjectMedicineen_US
dc.titlePlasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infanten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0347811687&origin=inwarden_US

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