APA

Taylor J. P., Metcalfe R. A., Watson P. F., Weetman A. P. & Trembath R. C. (20020425). Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. : The Journal of clinical endocrinology and metabolism.

Chicago

Taylor Julie P, Metcalfe Russell A, Watson Philip F, Weetman Anthony P and Trembath Richard C. 20020425. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. : The Journal of clinical endocrinology and metabolism.

Harvard

Taylor J. P., Metcalfe R. A., Watson P. F., Weetman A. P. and Trembath R. C. (20020425). Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. : The Journal of clinical endocrinology and metabolism.

MLA

Taylor Julie P, Metcalfe Russell A, Watson Philip F, Weetman Anthony P and Trembath Richard C. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. : The Journal of clinical endocrinology and metabolism. 20020425.