Monteiro, Fabiola P; Curry, Cynthia J; Hevner, Robert; Elliott, Stephen; Fisher, Jamie H; Turocy, John; Dobyns, William B; Costa, Larissa A; Freitas, Erika; Kitajima, Joao Paulo; Kok, Fernando 
Source: European journal of medical genetics. Unidade: FM
Subjects: ANORMALIDADES DO SISTEMA NERVOSO, ANORMALIDADES MUSCULOSQUELÉTICAS, ADENOSINA TRIFOSFATO, ERITROBLASTOSE FETAL, MICROCEFALIA, CÓRTEX CEREBRAL
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MONTEIRO, Fabiola P et al. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. European journal of medical genetics, v. 63, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2019.01.014. Acesso em: 14 nov. 2024.APA
Monteiro, F. P., Curry, C. J., Hevner, R., Elliott, S., Fisher, J. H., Turocy, J., et al. (2020). Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. European journal of medical genetics, 63( 1). doi:10.1016/j.ejmg.2019.01.014NLM
Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations [Internet]. European journal of medical genetics. 2020 ; 63( 1):[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmg.2019.01.014Vancouver
Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations [Internet]. European journal of medical genetics. 2020 ; 63( 1):[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmg.2019.01.014
