Source: Journal of Inherited Metabolic Disease. Unidade: FMRP
Assunto: DOENÇAS METABÓLICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WAJNER, M. et al. D-2-hydroxyglutaric aciduria in a patient with a severe clinical phenotype and anusual MRI findings. Journal of Inherited Metabolic Disease, v. 25, p. 28-34, 2002Tradução . . Acesso em: 29 maio 2024.APA
Wajner, M., Vargas, C. R., Funayama, C. A. R., Fernandez, A., ELIAS, M. L. C., Goodman, S. I., et al. (2002). D-2-hydroxyglutaric aciduria in a patient with a severe clinical phenotype and anusual MRI findings. Journal of Inherited Metabolic Disease, 25, 28-34.NLM
Wajner M, Vargas CR, Funayama CAR, Fernandez A, ELIAS MLC, Goodman SI, Jakobs C, Knaap MSVD. D-2-hydroxyglutaric aciduria in a patient with a severe clinical phenotype and anusual MRI findings. Journal of Inherited Metabolic Disease. 2002 ; 25 28-34.[citado 2024 maio 29 ]Vancouver
Wajner M, Vargas CR, Funayama CAR, Fernandez A, ELIAS MLC, Goodman SI, Jakobs C, Knaap MSVD. D-2-hydroxyglutaric aciduria in a patient with a severe clinical phenotype and anusual MRI findings. Journal of Inherited Metabolic Disease. 2002 ; 25 28-34.[citado 2024 maio 29 ]
