W, S., Y, C., N, I., K, Y., T, K., & K, N. (2024). Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1. Pediatric nephrology (Berlin, Germany), 39(8), 2351. https://doi.org/10.1007/s00467-024-06347-z
Chicago Style (17th ed.) CitationW, Shimabukuro, Chinen Y, Imanaga N, Yanagi K, Kaname T, and Nakanishi K. "Renal Coloboma Syndrome/dominant Optic Atrophy with Severe Retinal Atrophy and De Novo Digenic Mutations in PAX2 and OPA1." Pediatric Nephrology (Berlin, Germany) 39, no. 8 (2024): 2351. https://doi.org/10.1007/s00467-024-06347-z.
MLA (9th ed.) CitationW, Shimabukuro, et al. "Renal Coloboma Syndrome/dominant Optic Atrophy with Severe Retinal Atrophy and De Novo Digenic Mutations in PAX2 and OPA1." Pediatric Nephrology (Berlin, Germany), vol. 39, no. 8, 2024, p. 2351, https://doi.org/10.1007/s00467-024-06347-z.