Source: Arquivos brasileiros de endocrinologia e metabologia. Unidade: FM
Subjects: DIABETES MELLITUS (GENÉTICA), GENES, VASOPRESSINAS, GLÂNDULA PITUITÁRIA POSTERIOR
ABNT
MELO, Maria Edna de et al. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family. Arquivos brasileiros de endocrinologia e metabologia, v. 52, n. 8, p. 1272-1276, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302008000800011. Acesso em: 02 nov. 2025.APA
Melo, M. E. de, Marui, S., Brito, V. N. de, Mancini, M. C., Mendonça, B. B. de, & Knoepfelmacher, M. (2008). Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family. Arquivos brasileiros de endocrinologia e metabologia, 52( 8), 1272-1276. doi:10.1590/s0004-27302008000800011NLM
Melo ME de, Marui S, Brito VN de, Mancini MC, Mendonça BB de, Knoepfelmacher M. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2008 ; 52( 8): 1272-1276.[citado 2025 nov. 02 ] Available from: https://doi.org/10.1590/s0004-27302008000800011Vancouver
Melo ME de, Marui S, Brito VN de, Mancini MC, Mendonça BB de, Knoepfelmacher M. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene a brazilian family [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2008 ; 52( 8): 1272-1276.[citado 2025 nov. 02 ] Available from: https://doi.org/10.1590/s0004-27302008000800011

