LC-MS/MS Identification of Prolidase Deficiency: A Rare Cause of Infantile Hepatosplenomegaly

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Bibliographic Details
Published inClinical chemistry (Baltimore, Md.) Vol. 68; no. 3; pp. 478 - 480
Main Authors Taibi, Ludmia, Schlemmer, Dimitri, Bouchereau, Juliette, Causson, Claudine, Pichard, Samia, Bourrat, Emmanuelle, Melki, Isabelle, Schiff, Manuel, Benoist, Jean-François, Imbard, Apolline
Format Journal Article
LanguageEnglish
Published England Oxford University Press 04.03.2022
Subjects
Amino acids
Chemistry
Chromatography
Enzymes
Hospitals
Laboratories
Metabolism
Pediatrics
Plasma
Prolidase
Urine
inherited disorders
mass spectrometry
high-performance liquid chromatography
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ISSN0009-9147
1530-8561
1530-8561
DOI10.1093/clinchem/hvab208

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ISSN:0009-9147
1530-8561
1530-8561
DOI:10.1093/clinchem/hvab208