Genetic assessment in primary hyperoxaluria: why it matters.

Mandrile G, Beck B, Acquaviva C, Rumsby G, Deesker L, Garrelfs S, Gupta A, Bacchetta J, Groothoff J, OxalEurope Consortium/Erknet Guideline Workgroup On Hyperoxaluria

Open source

DOI: 10.1007/s00467-022-05613-2
Published: 2023 Mar
Container: Pediatric nephrology (Berlin, Germany)
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1007/s00467-022-05613-2,
  title = {Genetic assessment in primary hyperoxaluria: why it matters.},
  author = {Mandrile G and Beck B and Acquaviva C and Rumsby G and Deesker L and Garrelfs S and Gupta A and Bacchetta J and Groothoff J and OxalEurope Consortium/Erknet Guideline Workgroup On Hyperoxaluria},
  year = {2023},
  journal = {Pediatric nephrology (Berlin, Germany)},
  doi = {10.1007/s00467-022-05613-2},
  url = {https://doi.org/10.1007/s00467-022-05613-2}
}

RIS

TY  - JOUR
TI  - Genetic assessment in primary hyperoxaluria: why it matters.
AU  - Mandrile G
AU  - Beck B
AU  - Acquaviva C
AU  - Rumsby G
AU  - Deesker L
AU  - Garrelfs S
AU  - Gupta A
AU  - Bacchetta J
AU  - Groothoff J
AU  - OxalEurope Consortium/Erknet Guideline Workgroup On Hyperoxaluria
PY  - 2023
JO  - Pediatric nephrology (Berlin, Germany)
DO  - 10.1007/s00467-022-05613-2
UR  - https://doi.org/10.1007/s00467-022-05613-2
ER  -

APA

G, M., B, B., C, A., G, R., L, D., S, G., A, G., J, B., J, G., & Hyperoxaluria, O. C. G. W. O. (2023). Genetic assessment in primary hyperoxaluria: why it matters.. Pediatric nephrology (Berlin, Germany). https://doi.org/10.1007/s00467-022-05613-2

Source records

pubmed · retrieved 2026-09-25T03:28:12.738Z