Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: DISLIPIDEMIAS (PATOLOGIA), BIOLOGIA MOLECULAR, HIRSUTISMO (FISIOPATOLOGIA), TECIDO ADIPOSO (PATOLOGIA), IMAGEM POR RESSONÂNCIA MAGNÉTICA, FENÓTIPOS (ANÁLISE), MUTAÇÃO GENÉTICA, INSULINA (RESISTÊNCIA)
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KIM, C. A. et al. Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 4, p. 1129-1134, 2008Tradução . . Disponível em: https://doi.org/10.1210/jc.2007-1328. Acesso em: 11 nov. 2024.APA
Kim, C. A., Delépine, M., Boutet, E., El Mourabit, H., Lay, S. L., Meier, M., et al. (2008). Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy. Journal of Clinical Endocrinology and Metabolism, 93( 4), 1129-1134. doi:10.1210/jc.2007-1328NLM
Kim CA, Delépine M, Boutet E, El Mourabit H, Lay SL, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O’Rahilly S, Dugail I, Capeau J, Lathrop M, Magre J. Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 4): 1129-1134.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1210/jc.2007-1328Vancouver
Kim CA, Delépine M, Boutet E, El Mourabit H, Lay SL, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O’Rahilly S, Dugail I, Capeau J, Lathrop M, Magre J. Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 4): 1129-1134.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1210/jc.2007-1328
