Source: Annals of human genetics. Unidade: FM
Subjects: SURDEZ, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
ABNT
SAMPAIO-SILVA, Juliana e BENTO, Ricardo Ferreira. Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family. Annals of human genetics, v. 82, n. 1, p. 23-34, 2018Tradução . . Disponível em: https://doi.org/10.1111/ahg.12213. Acesso em: 10 set. 2024.APA
Sampaio-silva, J., & Bento, R. F. (2018). Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family. Annals of human genetics, 82( 1), 23-34. doi:10.1111/ahg.12213NLM
Sampaio-silva J, Bento RF. Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family [Internet]. Annals of human genetics. 2018 ; 82( 1): 23-34.[citado 2024 set. 10 ] Available from: https://doi.org/10.1111/ahg.12213Vancouver
Sampaio-silva J, Bento RF. Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family [Internet]. Annals of human genetics. 2018 ; 82( 1): 23-34.[citado 2024 set. 10 ] Available from: https://doi.org/10.1111/ahg.12213