Source: Frontiers in endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, PUBERDADE, FENÓTIPOS, DOENÇAS GENÉTICAS
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MONTENEGRO JUNIOR, Renan Magalhaes e JORGE, Alexander Augusto de Lima. Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred. Frontiers in endocrinology, v. 9, 2018Tradução . . Disponível em: https://doi.org/10.3389/fendo.2018.00458. Acesso em: 08 maio 2024.APA
Montenegro Junior, R. M., & Jorge, A. A. de L. (2018). Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred. Frontiers in endocrinology, 9. doi:10.3389/fendo.2018.00458NLM
Montenegro Junior RM, Jorge AA de L. Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred [Internet]. Frontiers in endocrinology. 2018 ; 9[citado 2024 maio 08 ] Available from: https://doi.org/10.3389/fendo.2018.00458Vancouver
Montenegro Junior RM, Jorge AA de L. Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred [Internet]. Frontiers in endocrinology. 2018 ; 9[citado 2024 maio 08 ] Available from: https://doi.org/10.3389/fendo.2018.00458
