The detection of abnormal metabolites in MCAD deficiency: a new method

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Published inJournal of inherited metabolic disease Vol. 13; no. 3; p. 315
Main Authors Blom, W, Polder-Mol, A C, Kelholt-Dijkman, H H, Hierck, L, Huijmans, J G
Format Journal Article
LanguageEnglish
Published United States 01.05.1990
Subjects
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Author Kelholt-Dijkman, H H
Huijmans, J G
Polder-Mol, A C
Blom, W
Hierck, L
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  fullname: Huijmans, J G
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crossref_primary_10_1007_BF00710286
crossref_primary_10_1016_S0009_8981_00_00195_9
crossref_primary_10_1007_BF00806075
crossref_primary_10_1080_10826079508009323
crossref_primary_10_1023_A_1005482828392
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PublicationTitle Journal of inherited metabolic disease
PublicationTitleAlternate J Inherit Metab Dis
PublicationYear 1990
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StartPage 315
SubjectTerms Acyl-CoA Dehydrogenase
Amino Acids - urine
Chromatography, Gas
Fatty Acid Desaturases - deficiency
Glutamates - urine
Glutamic Acid
Glutamine - urine
Glycine - urine
Humans
Mass Spectrometry
Piperidones - urine
Title The detection of abnormal metabolites in MCAD deficiency: a new method
URI https://www.ncbi.nlm.nih.gov/pubmed/1977955
Volume 13
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