APA

Dias A. M. M., Lezirovitz K., Nicastro F. S., Mendes B. C. A. & Mingroni-Netto R. C. (20190410). Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. : Journal of human genetics.

Chicago

Dias Alex Marcel Moreira, Lezirovitz Karina, Nicastro Fernanda Stávale, Mendes Beatriz C A and Mingroni-Netto Regina Célia. 20190410. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. : Journal of human genetics.

Harvard

Dias A. M. M., Lezirovitz K., Nicastro F. S., Mendes B. C. A. and Mingroni-Netto R. C. (20190410). Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. : Journal of human genetics.

MLA

Dias Alex Marcel Moreira, Lezirovitz Karina, Nicastro Fernanda Stávale, Mendes Beatriz C A and Mingroni-Netto Regina Célia. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. : Journal of human genetics. 20190410.