Publisher Correction: Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2...Hashmi S, Khatri S, Qaiser H, et al. Pediatric Nephrology. 2026;41(7):2033-2041.

This publisher correction addresses an error in a previously published article in Pediatric Nephrology, where the captions for Figures 3 and 4 were mistakenly swapped. The original article has been updated to correct this mistake. The publisher also notes neutrality regarding jurisdictional claims i...

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Detalles Bibliográficos
Publicado en:Pediatric Nephrology Vol. 41; no. 7; pp. 2299 - 2300
Autores principales: Hashmi, Seema, Khatri, Sabeeta, Qaiser, Habib, Abid, Aiysha, Firasat, Sadaf, Sultan, Sajid, Zubair, Aasia, Zafar, Mirza Naqi, Ahmed, Bashir, Umer, Sadaf Aba, Rizvi, Syed Adibul Hasan, Ali, Irshad
Formato: corrected article Journal Article
Publicado: Springer Nature Jul2026
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:This publisher correction addresses an error in a previously published article in Pediatric Nephrology, where the captions for Figures 3 and 4 were mistakenly swapped. The original article has been updated to correct this mistake. The publisher also notes neutrality regarding jurisdictional claims in maps and institutional affiliations.