Source: The Journal of Clinical Endocrinology and Metabolism. Unidade: ICB
Assunto: FISIOLOGIA
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NICOLA, Juan Pablo et al. Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5' -untranslated region in a patient with congenital hypothyroidism. The Journal of Clinical Endocrinology and Metabolism, v. 96, n. 7, p. E1100-E1107, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-0349. Acesso em: 01 set. 2024.APA
Nicola, J. P., Nazar, M., Serrano-Nascimento, C., Silva, F. G. da, Sobrero, G., Testa, G., et al. (2011). Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5' -untranslated region in a patient with congenital hypothyroidism. The Journal of Clinical Endocrinology and Metabolism, 96( 7), E1100-E1107. doi:10.1210/jc.2011-0349NLM
Nicola JP, Nazar M, Serrano-Nascimento C, Silva FG da, Sobrero G, Testa G, Nunes MT, Muñoz L, Miras M, Masini-Repiso AM. Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5' -untranslated region in a patient with congenital hypothyroidism [Internet]. The Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 7): E1100-E1107.[citado 2024 set. 01 ] Available from: https://doi.org/10.1210/jc.2011-0349Vancouver
Nicola JP, Nazar M, Serrano-Nascimento C, Silva FG da, Sobrero G, Testa G, Nunes MT, Muñoz L, Miras M, Masini-Repiso AM. Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5' -untranslated region in a patient with congenital hypothyroidism [Internet]. The Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 7): E1100-E1107.[citado 2024 set. 01 ] Available from: https://doi.org/10.1210/jc.2011-0349