APA

Uehara D. T., Freitas É. L., Alves L. U., Mazzeu J. F., Auricchio M. T., Tabith A., Monteiro M. L., Rosenberg C. & Mingroni-Netto R. C. (20160415). A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. : Human genome variation.

Chicago

Uehara Daniela T, Freitas Érika L, Alves Leandro U, Mazzeu Juliana F, Auricchio Maria Tbm, Tabith Alfredo, Monteiro Mário Lr, Rosenberg Carla and Mingroni-Netto Regina C. 20160415. A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. : Human genome variation.

Harvard

Uehara D. T., Freitas É. L., Alves L. U., Mazzeu J. F., Auricchio M. T., Tabith A., Monteiro M. L., Rosenberg C. and Mingroni-Netto R. C. (20160415). A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. : Human genome variation.

MLA

Uehara Daniela T, Freitas Érika L, Alves Leandro U, Mazzeu Juliana F, Auricchio Maria Tbm, Tabith Alfredo, Monteiro Mário Lr, Rosenberg Carla and Mingroni-Netto Regina C. A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. : Human genome variation. 20160415.