Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? (2018)
Ceroni, José R. M; Yamamoto, Guilherme L; Honjo, Rachel S; Kim, Chong A; Passos-Bueno, Maria Rita 
; Bertola, Débora R
Source: Genetics and Molecular Biology. Unidades: FM, IB
Subjects: GENÉTICA MÉDICA, MUTAÇÃO GENÉTICA, ENZIMAS, DIAGNÓSTICO CLÍNICO
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CERONI, José R. M et al. Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?. Genetics and Molecular Biology, 2018Tradução . . Disponível em: https://doi.org/10.1590/1678-4685-gmb-2017-0172. Acesso em: 30 jun. 2024.APA
Ceroni, J. R. M., Yamamoto, G. L., Honjo, R. S., Kim, C. A., Passos-Bueno, M. R., & Bertola, D. R. (2018). Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? Genetics and Molecular Biology. doi:10.1590/1678-4685-gmb-2017-0172NLM
Ceroni JRM, Yamamoto GL, Honjo RS, Kim CA, Passos-Bueno MR, Bertola DR. Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? [Internet]. Genetics and Molecular Biology. 2018 ;[citado 2024 jun. 30 ] Available from: https://doi.org/10.1590/1678-4685-gmb-2017-0172Vancouver
Ceroni JRM, Yamamoto GL, Honjo RS, Kim CA, Passos-Bueno MR, Bertola DR. Large deletion in PIGL: a common mutational mechanism in CHIME syndrome? [Internet]. Genetics and Molecular Biology. 2018 ;[citado 2024 jun. 30 ] Available from: https://doi.org/10.1590/1678-4685-gmb-2017-0172
