Source: Resumos. Conference titles: Workshop do Programa de Pós-Graduação em Genética da FMRP-USP. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, FENÓTIPOS
ABNT
GRANGEIRO, C. H. P. e HUBER, Jair e MARTELLI, Lúcia Regina. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. 2017, Anais.. Ribeirão Preto: FMRP-USP, 2017. . Acesso em: 31 out. 2024.APA
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. In Resumos. Ribeirão Preto: FMRP-USP.NLM
Grangeiro CHP, Huber J, Martelli LR. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. Resumos. 2017 ;[citado 2024 out. 31 ]Vancouver
Grangeiro CHP, Huber J, Martelli LR. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. Resumos. 2017 ;[citado 2024 out. 31 ]