A novel nonsense mutation in the mineralocorticoid receptor gene in a family with a renal form od type 1 pseudohypoaldosteronism (PHA-1) (2004)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MARTINELLI JUNIOR, CARLOS EDUARDO - FMRP
- Unidade: FMRP
- Subjects: ENDOCRINOLOGIA; PEDIATRIA
- Language: Inglês
- Imprenta:
- Publisher: International Society of Endocrinology
- Publisher place: London
- Date published: 2004
- Source:
- Título: Programa and Abstracts
- Conference titles: International Congress of Endocronology
-
ABNT
FERNANDES ROSA, F. L. et al. A novel nonsense mutation in the mineralocorticoid receptor gene in a family with a renal form od type 1 pseudohypoaldosteronism (PHA-1). 2004, Anais.. London: International Society of Endocrinology, 2004. . Acesso em: 28 dez. 2025. -
APA
Fernandes Rosa, F. L., Faria, C., Santos, P. V., Elias, L. L., Castro, M. de, Martinelli Júnior, C. E., & Antonini, S. R. (2004). A novel nonsense mutation in the mineralocorticoid receptor gene in a family with a renal form od type 1 pseudohypoaldosteronism (PHA-1). In Programa and Abstracts. London: International Society of Endocrinology. -
NLM
Fernandes Rosa FL, Faria C, Santos PV, Elias LL, Castro M de, Martinelli Júnior CE, Antonini SR. A novel nonsense mutation in the mineralocorticoid receptor gene in a family with a renal form od type 1 pseudohypoaldosteronism (PHA-1). Programa and Abstracts. 2004 ;[citado 2025 dez. 28 ] -
Vancouver
Fernandes Rosa FL, Faria C, Santos PV, Elias LL, Castro M de, Martinelli Júnior CE, Antonini SR. A novel nonsense mutation in the mineralocorticoid receptor gene in a family with a renal form od type 1 pseudohypoaldosteronism (PHA-1). Programa and Abstracts. 2004 ;[citado 2025 dez. 28 ] - Hiperparatireoidismo como primeira manifestação de NEM tipo-HA em criança carregadora da mutação C634R no proto-oncogene RET
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