Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? (2018)
Source: Genetics and Molecular Biology. Unidade: FM
Subjects: SEQUENCIAMENTO GENÉTICO, RETÍCULO ENDOPLASMÁTICO, MUTAÇÃO GENÉTICA, SINAIS E SINTOMAS
ABNT
CERONI, Jose R. M. et al. Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?. Genetics and Molecular Biology, v. 41, n. 1, p. 85-91, 2018Tradução . . Disponível em: https://doi.org/10.1590/1678-4685-GMB-2017-0172. Acesso em: 09 out. 2024.APA
Ceroni, J. R. M., Kim, C. A., Yamamoto, G. L., Honjo, R. S., Passos-Bueno, M. R., & Bertola, D. R. (2018). Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? Genetics and Molecular Biology, 41( 1), 85-91. doi:10.1590/1678-4685-GMB-2017-0172NLM
Ceroni JRM, Kim CA, Yamamoto GL, Honjo RS, Passos-Bueno MR, Bertola DR. Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? [Internet]. Genetics and Molecular Biology. 2018 ; 41( 1): 85-91.[citado 2024 out. 09 ] Available from: https://doi.org/10.1590/1678-4685-GMB-2017-0172Vancouver
Ceroni JRM, Kim CA, Yamamoto GL, Honjo RS, Passos-Bueno MR, Bertola DR. Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? [Internet]. Genetics and Molecular Biology. 2018 ; 41( 1): 85-91.[citado 2024 out. 09 ] Available from: https://doi.org/10.1590/1678-4685-GMB-2017-0172