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Genetic assessment in primary hyperoxaluria: why it matters:
Mandrile, Giorgia
;
Beck, Bodo
;
Acquaviva, Cecile
...
Pediatric Nephrology. 38 (2022) 3 - p. 625-634 , 2022
Link:
https://doi.org/10.1007/s00467-022-05613-2
RT Journal T1
Genetic assessment in primary hyperoxaluria: why it matters
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s00467-022-05613-2&Exemplar=1&LAN=DE A1 Mandrile, Giorgia A1 Beck, Bodo A1 Acquaviva, Cecile A1 Rumsby, Gill A1 Deesker, Lisa A1 Garrelfs, Sander A1 Gupta, Asheeta A1 Bacchetta, Justine A1 Groothoff, Jaap A1 on behalf of the OxalEurope Consortium/Erknet Guideline Workgroup On Hyperoxaluria PB Springer Science and Business Media LLC YR 2022 SN 0931-041X SN 1432-198X JF Pediatric Nephrology VO 38 IS 3 SP 625 OP 634 LK http://dx.doi.org/https://doi.org/10.1007/s00467-022-05613-2 DO https://doi.org/10.1007/s00467-022-05613-2 SF ELIB - SuUB Bremen
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