Genetic Investigation of Regulatory Regions of MKRN3 and DLK1 Genes in Children with Central Precocious Puberty
Pathogenic variants in the regulatory region of MKRN3 gene are rare and can be associated with the CPP phenotype.
Authors
- Ana Cláudia Latronico (ORCID: https://orcid.org/0000-0001-6782-693X)
- Berenice B. Mendonça (ORCID: https://orcid.org/0000-0003-1762-1084)
- Maiara Ribeiro Piovesan (ORCID: https://orcid.org/0009-0002-0112-4657)
- Luciana Ribeiro Montenegro
- Larissa Baracho Macena
- Vinícius Nahime Brito (ORCID: https://orcid.org/0000-0002-1052-2246)
- Helena Panteliou Lima‐Valassi
- Ana Pinheiro Machado Canton (ORCID: https://orcid.org/0000-0001-8662-5412)
- Alexander A.L. Jorge (ORCID: https://orcid.org/0000-0003-2567-7360)
Institutions
- Universidade de São Paulo (BR)
- Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR)
Publication Details
- Journal
- Hormone Research in Paediatrics
- Published
- 2024-12-20
- DOI
- https://doi.org/10.1159/000543155
- Primary Topic
- Nuclear Structure and Function
- Type
- article
- Field-Weighted Citation Impact
- 0.00