A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus (2004)
- Autores:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assuntos: GENÓTIPOS (ANORMALIDADES); DIABETES INSÍPIDO (GENÉTICA); BRASILEIROS (GENÉTICA; SEQUENCIAMENTO GENÉTICO
- Idioma: Inglês
- Imprenta:
- Editora: International Society of Endocrinology
- Local: Lisboa
- Data de publicação: 2004
- Fonte:
- Título do periódico: Program and Abstracts
- Nome do evento: International Congress of Endocrinology
-
ABNT
MELO, M. E. et al. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 23 abr. 2024. -
APA
Melo, M. E., Marui, S., Mendonca, B. B., & Knoepfelmacher, M. (2004). A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. In Program and Abstracts. Lisboa: International Society of Endocrinology. -
NLM
Melo ME, Marui S, Mendonca BB, Knoepfelmacher M. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. Program and Abstracts. 2004 ;[citado 2024 abr. 23 ] -
Vancouver
Melo ME, Marui S, Mendonca BB, Knoepfelmacher M. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. Program and Abstracts. 2004 ;[citado 2024 abr. 23 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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