Source: Journal of Inborn Errors of Metabolism and Screening. Conference titles: International Congress on Inborn Errors of Metabolism (ICIEM). Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, FENÓTIPOS
ABNT
GRANGEIRO, Carlos Henrique Paiva e HUBER, Jair e MARTELLI, Lúcia Regina. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two Brazilians siblings. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1177/2326409817722292. Acesso em: 30 maio 2024. , 2017APA
Grangeiro, C. H. P., Huber, J., & Martelli, L. R. (2017). Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two Brazilians siblings. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1177/2326409817722292NLM
Grangeiro CHP, Huber J, Martelli LR. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two Brazilians siblings [Internet]. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5( sep): 146.[citado 2024 maio 30 ] Available from: https://doi.org/10.1177/2326409817722292Vancouver
Grangeiro CHP, Huber J, Martelli LR. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two Brazilians siblings [Internet]. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5( sep): 146.[citado 2024 maio 30 ] Available from: https://doi.org/10.1177/2326409817722292