Cite
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease
MLA
Adrian S. Woolf, et al. “A Homozygous Missense Variant in CHRM3 Associated with Familial Urinary Bladder Disease.” Clinical Genetics, vol. 96, no. 6, Sept. 2019, pp. 515–20. EBSCOhost, https://doi.org/10.1111/cge.13631.
APA
Adrian S. Woolf, William G. Newman, Ali Aishah, Katherine A. Wood, Raymond T. O’Keefe, Jill E. Urquhart, Glenda M. Beaman, Sanjeev S. Bhaskar, Gabriella Galatà, Helen M. Stuart, Keng Wee Teik, James O’Sullivan, & Huw B. Thomas. (2019). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical Genetics, 96(6), 515–520. https://doi.org/10.1111/cge.13631
Chicago
Adrian S. Woolf, William G. Newman, Ali Aishah, Katherine A. Wood, Raymond T. O’Keefe, Jill E. Urquhart, Glenda M. Beaman, et al. 2019. “A Homozygous Missense Variant in CHRM3 Associated with Familial Urinary Bladder Disease.” Clinical Genetics 96 (6): 515–20. doi:10.1111/cge.13631.