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LC-MS/MS Identification of Prolidase Deficiency: A Rare Cau..:
Taibi, Ludmia
;
Schlemmer, Dimitri
;
Bouchereau, Juliette
...
Clinical Chemistry. 68 (2022) 3 - p. 478-480 , 2022
Link:
https://doi.org/10.1093/clinchem/hvab208
RT Journal T1
LC-MS/MS Identification of Prolidase Deficiency: A Rare Cause of Infantile Hepatosplenomegaly
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_clinchem_hvab208&Exemplar=1&LAN=DE A1 Taibi, Ludmia A1 Schlemmer, Dimitri A1 Bouchereau, Juliette A1 Causson, Claudine A1 Pichard, Samia A1 Bourrat, Emmanuelle A1 Melki, Isabelle A1 Schiff, Manuel A1 Benoist, Jean-François A1 Imbard, Apolline PB Oxford University Press (OUP) YR 2022 SN 0009-9147 SN 1530-8561 JF Clinical Chemistry VO 68 IS 3 SP 478 OP 480 LK http://dx.doi.org/https://doi.org/10.1093/clinchem/hvab208 DO https://doi.org/10.1093/clinchem/hvab208 SF ELIB - SuUB Bremen
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