Farias, Allysson Allan de; Nunes, Kelly; Lemes, Renan Barbosa; Moura, Ronald; Fernandes, Gustavo Ribeiro; Melo, Uira Souto; Zatz, Mayana 
; Kok, Fernando; Santos, Silvana
Source: Scientific reports. Unidade: FM
Subjects: DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, GENEALOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FARIAS, Allysson Allan de et al. Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations. Scientific reports, v. 8, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-35022-1. Acesso em: 19 nov. 2024.APA
Farias, A. A. de, Nunes, K., Lemes, R. B., Moura, R., Fernandes, G. R., Melo, U. S., et al. (2018). Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations. Scientific reports, 8. doi:10.1038/s41598-018-35022-1NLM
Farias AA de, Nunes K, Lemes RB, Moura R, Fernandes GR, Melo US, Zatz M, Kok F, Santos S. Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations [Internet]. Scientific reports. 2018 ; 8[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-018-35022-1Vancouver
Farias AA de, Nunes K, Lemes RB, Moura R, Fernandes GR, Melo US, Zatz M, Kok F, Santos S. Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations [Internet]. Scientific reports. 2018 ; 8[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-018-35022-1
