Source: Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: CRIANÇAS, ADULTOS, MUTAÇÃO GENÉTICA, GLICOPROTEÍNAS, HIPOTIREOIDISMO (CONGÊNITO), GENÓTIPOS
ABNT
PARDO, Viviane et al. The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation. Journal of Clinical Endocrinology & Metabolism, v. 94, n. 8, p. 2938-2944, 2009Tradução . . Disponível em: https://doi.org/10.1210/jc.2009-0150. Acesso em: 17 out. 2024.APA
Pardo, V., Vono-Toniolo, J., Rubio, I. G. S., Knobel, M., Possato, R. F., Targovnik, H. M., et al. (2009). The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation. Journal of Clinical Endocrinology & Metabolism, 94( 8), 2938-2944. doi:10.1210/jc.2009-0150NLM
Pardo V, Vono-Toniolo J, Rubio IGS, Knobel M, Possato RF, Targovnik HM, Kopp P, Medeiros-Neto G. The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation [Internet]. Journal of Clinical Endocrinology & Metabolism. 2009 ; 94( 8): 2938-2944.[citado 2024 out. 17 ] Available from: https://doi.org/10.1210/jc.2009-0150Vancouver
Pardo V, Vono-Toniolo J, Rubio IGS, Knobel M, Possato RF, Targovnik HM, Kopp P, Medeiros-Neto G. The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation [Internet]. Journal of Clinical Endocrinology & Metabolism. 2009 ; 94( 8): 2938-2944.[citado 2024 out. 17 ] Available from: https://doi.org/10.1210/jc.2009-0150