APA

Wesdorp M., Schreur V., Beynon A. J., Oostrik J., van de Kamp J. M., Elting M. W., van den Boogaard M. H., Feenstra I., Admiraal R. J. C., Kunst H. P. M., Hoyng C. B., Kremer H., Yntema H. G., Pennings R. J. E. & Schraders M. (20191115). Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. : Clinical genetics.

Chicago

Wesdorp M, Schreur V, Beynon A J, Oostrik J, van de Kamp J M, Elting M W, van den Boogaard M-J H, Feenstra I, Admiraal R J C, Kunst H P M, Hoyng C B, Kremer H, Yntema H G, Pennings R J E and Schraders M. 20191115. Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. : Clinical genetics.

Harvard

Wesdorp M., Schreur V., Beynon A. J., Oostrik J., van de Kamp J. M., Elting M. W., van den Boogaard M. H., Feenstra I., Admiraal R. J. C., Kunst H. P. M., Hoyng C. B., Kremer H., Yntema H. G., Pennings R. J. E. and Schraders M. (20191115). Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. : Clinical genetics.

MLA

Wesdorp M, Schreur V, Beynon A J, Oostrik J, van de Kamp J M, Elting M W, van den Boogaard M-J H, Feenstra I, Admiraal R J C, Kunst H P M, Hoyng C B, Kremer H, Yntema H G, Pennings R J E and Schraders M. Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. : Clinical genetics. 20191115.