Hashmi, S., Khatri, S., Qaiser, H., Abid, A., Firasat, S., Sultan, S., . . . Ali, I. (2026). 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. Pediatric Nephrology, 41(7), 2299-2300.
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Cita Chicago Style (17a ed.)
Hashmi, Seema, et al. "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."
Pediatric Nephrology 41, no. 7 (2026): 2299-2300.
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Cita MLA (9a ed.)
Hashmi, Seema, et al. "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."
Pediatric Nephrology, vol. 41, no. 7, 2026, pp. 2299-2300.
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