APA (7th ed.) Citation

GM, B., G, G., KW, T., JE, U., A, A., J, O., . . . WG, N. (2019). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical genetics, 96(6), 515. https://doi.org/10.1111/cge.13631

Chicago Style (17th ed.) Citation

GM, Beaman, et al. "A Homozygous Missense Variant in CHRM3 Associated with Familial Urinary Bladder Disease." Clinical Genetics 96, no. 6 (2019): 515. https://doi.org/10.1111/cge.13631.

MLA (9th ed.) Citation

GM, Beaman, et al. "A Homozygous Missense Variant in CHRM3 Associated with Familial Urinary Bladder Disease." Clinical Genetics, vol. 96, no. 6, 2019, p. 515, https://doi.org/10.1111/cge.13631.