Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger (1993)
- Authors:
- USP affiliated authors: WAJCHENBERG, BERNARDO LEO - FM ; MEDEIROS NETO, GERALDO ANTONIO DE - FM
- Unidade: FM
- DOI: 10.1210/jcem.77.1.8325944
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Clinical Endocrinology and Metabolism
- Volume/Número/Paginação/Ano: v.77, n.1 , p.210-5, jul. 1993
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
TARGOVNIK, H M et al. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism, v. 77, n. 1 , p. 210-5, 1993Tradução . . Disponível em: https://doi.org/10.1210/jcem.77.1.8325944. Acesso em: 01 jun. 2024. -
APA
Targovnik, H. M., Medeiros Neto, G. A., Varela, V., Cochaux, P., Wajchenberg, B. L., & Vassart, G. (1993). Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism, 77( 1 ), 210-5. doi:10.1210/jcem.77.1.8325944 -
NLM
Targovnik HM, Medeiros Neto GA, Varela V, Cochaux P, Wajchenberg BL, Vassart G. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger [Internet]. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1210/jcem.77.1.8325944 -
Vancouver
Targovnik HM, Medeiros Neto GA, Varela V, Cochaux P, Wajchenberg BL, Vassart G. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger [Internet]. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1210/jcem.77.1.8325944 - Effect of hypocaloric diet with and without d-fenfluramine treatment on growth hormone release after growth hormone-releasing factor stimulation in patients with android obesity
- Hyposialylated thyroglobulin in a patient with congenital goiter and hypothyroidism
- 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis
- Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin
- Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism
- Genetic linkage studies of thyroid peroxidase (tpo) gene in families with tpo deficiency
- Defective organification of iodice causing hereditary goitrous hypothyroidism
- Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism
- Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis
- Human thyroid tissue do not express thyroalbumin
Informações sobre o DOI: 10.1210/jcem.77.1.8325944 (Fonte: oaDOI API)
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