APA

Beaman G. M., Galatà G., Teik K. W., Urquhart J. E., Aishah A., O'Sullivan J., Bhaskar S. S., Wood K. A., Thomas H. B., O'Keefe R. T., Woolf A. S., Stuart H. M. & Newman W. G. (20200831). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. : Clinical genetics.

Chicago

Beaman Glenda M, Galatà Gabriella, Teik Keng W, Urquhart Jill E, Aishah Ali, O'Sullivan James, Bhaskar Sanjeev S, Wood Katherine A, Thomas Huw B, O'Keefe Raymond T, Woolf Adrian S, Stuart Helen M and Newman William G. 20200831. A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. : Clinical genetics.

Harvard

Beaman G. M., Galatà G., Teik K. W., Urquhart J. E., Aishah A., O'Sullivan J., Bhaskar S. S., Wood K. A., Thomas H. B., O'Keefe R. T., Woolf A. S., Stuart H. M. and Newman W. G. (20200831). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. : Clinical genetics.

MLA

Beaman Glenda M, Galatà Gabriella, Teik Keng W, Urquhart Jill E, Aishah Ali, O'Sullivan James, Bhaskar Sanjeev S, Wood Katherine A, Thomas Huw B, O'Keefe Raymond T, Woolf Adrian S, Stuart Helen M and Newman William G. A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. : Clinical genetics. 20200831.