Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip Congenital ludoystrophy and brunzell syndrome: phenotype variability suggest important modifier effects (2003)
- Autores:
- Autor USP: WAJCHENBERG, BERNARDO LEO - FM
- Unidade: FM
- Assuntos: MUTAÇÃO GENÉTICA; FENÓTIPOS; DOENCAS (CONGÊNITO)
- Idioma: Inglês
- Fonte:
- Título do periódico: The Journal of Clinical Endocrinology & Metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 89, n. 6, p. 2916-2922, 2003
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ABNT
FU, Mao et al. Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip Congenital ludoystrophy and brunzell syndrome: phenotype variability suggest important modifier effects. The Journal of Clinical Endocrinology & Metabolism, v. 89, n. 6, p. 2916-2922, 2003Tradução . . Acesso em: 24 abr. 2024. -
APA
Fu, M., Kazlauskaite, R., Baracho, M. de F. P., Santos, M. G. do, Brandão Neto, J., Villares, S., et al. (2003). Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip Congenital ludoystrophy and brunzell syndrome: phenotype variability suggest important modifier effects. The Journal of Clinical Endocrinology & Metabolism, 89( 6), 2916-2922. -
NLM
Fu M, Kazlauskaite R, Baracho M de FP, Santos MG do, Brandão Neto J, Villares S, Celi FS, Wajchenberg BL, Shuldiner AR. Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip Congenital ludoystrophy and brunzell syndrome: phenotype variability suggest important modifier effects. The Journal of Clinical Endocrinology & Metabolism. 2003 ; 89( 6): 2916-2922.[citado 2024 abr. 24 ] -
Vancouver
Fu M, Kazlauskaite R, Baracho M de FP, Santos MG do, Brandão Neto J, Villares S, Celi FS, Wajchenberg BL, Shuldiner AR. Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip Congenital ludoystrophy and brunzell syndrome: phenotype variability suggest important modifier effects. The Journal of Clinical Endocrinology & Metabolism. 2003 ; 89( 6): 2916-2922.[citado 2024 abr. 24 ] - Bone involvement in idiopathic hypercalciuria
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