Source: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, FENÓTIPOS, DOENCAS (CONGÊNITO)
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: 19 out. 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 out. 19 ]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 out. 19 ]