APA (7th ed.) Citation

E, G., A, W., JS, P., PYB, A., FP, B., RE, L., & AM, I. (2024). Genome sequencing identifies biallelic variants in SCLT1 in a patient with syndromic nephronophthisis: Reflections on the SCLT1-related ciliopathy spectrum. American journal of medical genetics. Part A, 194(11), e63789. https://doi.org/10.1002/ajmg.a.63789

Chicago Style (17th ed.) Citation

E, Gillesse, Wade A, Parboosingh JS, Au PYB, Bernier FP, Lamont RE, and Innes AM. "Genome Sequencing Identifies Biallelic Variants in SCLT1 in a Patient with Syndromic Nephronophthisis: Reflections on the SCLT1-related Ciliopathy Spectrum." American Journal of Medical Genetics. Part A 194, no. 11 (2024): e63789. https://doi.org/10.1002/ajmg.a.63789.

MLA (9th ed.) Citation

E, Gillesse, et al. "Genome Sequencing Identifies Biallelic Variants in SCLT1 in a Patient with Syndromic Nephronophthisis: Reflections on the SCLT1-related Ciliopathy Spectrum." American Journal of Medical Genetics. Part A, vol. 194, no. 11, 2024, p. e63789, https://doi.org/10.1002/ajmg.a.63789.