APA (7th ed.) Citation

V, C., M, R., P, A., C, M., J, P., N, C., . . . L, F. T. (2024). Homozygosity for a hypomorphic mutation in frizzled class receptor 5 causes syndromic ocular coloboma with microcornea in humans. Human genetics, 143(12), 1509. https://doi.org/10.1007/s00439-024-02712-y

Chicago Style (17th ed.) Citation

V, Cortés-González, et al. "Homozygosity for a Hypomorphic Mutation in Frizzled Class Receptor 5 Causes Syndromic Ocular Coloboma with Microcornea in Humans." Human Genetics 143, no. 12 (2024): 1509. https://doi.org/10.1007/s00439-024-02712-y.

MLA (9th ed.) Citation

V, Cortés-González, et al. "Homozygosity for a Hypomorphic Mutation in Frizzled Class Receptor 5 Causes Syndromic Ocular Coloboma with Microcornea in Humans." Human Genetics, vol. 143, no. 12, 2024, p. 1509, https://doi.org/10.1007/s00439-024-02712-y.