APA (7th ed.) Citation

W, L., GH, C., NN, L., JY, L., YQ, T., JS, L., & LL, F. (2026). Whole exome sequencing identified a novel compound heterozygous mutation of nephrocystin 4 in a child with nephronophthisis-a rare case report. Frontiers in pediatrics, 14, 1864993. https://doi.org/10.3389/fped.2026.1864993

Chicago Style (17th ed.) Citation

W, Li, Cao GH, Li NN, Long JY, Tang YQ, Liu JS, and Fan LL. "Whole Exome Sequencing Identified a Novel Compound Heterozygous Mutation of Nephrocystin 4 in a Child with Nephronophthisis-a Rare Case Report." Frontiers in Pediatrics 14 (2026): 1864993. https://doi.org/10.3389/fped.2026.1864993.

MLA (9th ed.) Citation

W, Li, et al. "Whole Exome Sequencing Identified a Novel Compound Heterozygous Mutation of Nephrocystin 4 in a Child with Nephronophthisis-a Rare Case Report." Frontiers in Pediatrics, vol. 14, 2026, p. 1864993, https://doi.org/10.3389/fped.2026.1864993.