EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome (2025)
- Authors:
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; HADDAD, LUCIANA AMARAL - IB ; BERTOLA, DÉBORA ROMEO - IB ; ROSENBERG, CARLA - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; CARVALHO, LAURA MACHADO LARA - IB ; BRANCO, ELISA VARELLA - IB ; OLIVEIRA, DANYLLO FELIPE DE - IB
- Unidades: FM; IB
- DOI: 10.1007/s12035-024-04655-x
- Subjects: GENÉTICA MÉDICA; MUTAÇÃO GENÉTICA; GENES
- Agências de fomento:
- Language: Inglês
- Sustainable Development Goals (GDS):
03. Good health and well-being
- Imprenta:
- Publisher place: Heidelberg
- Date published: 2025
- Source:
- Título: Molecular Neurobiology
- ISSN: 1559-1182
- Volume/Número/Paginação/Ano: v. 62, p. 5977–5989, 2025
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
CARVALHO, Laura Machado Lara et al. EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome. Molecular Neurobiology, v. 62, p. 5977–5989, 2025Tradução . . Disponível em: https://doi.org/10.1007/s12035-024-04655-x. Acesso em: 28 dez. 2025. -
APA
Carvalho, L. M. L., Jorge, A. A. de L., Branco, E. V., Oliveira, D. F. de, Haddad, L. A., Bertola, D. R., et al. (2025). EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome. Molecular Neurobiology, 62, 5977–5989. doi:10.1007/s12035-024-04655-x -
NLM
Carvalho LML, Jorge AA de L, Branco EV, Oliveira DF de, Haddad LA, Bertola DR, Rosenberg C, Krepischi ACV. EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome [Internet]. Molecular Neurobiology. 2025 ; 62 5977–5989.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1007/s12035-024-04655-x -
Vancouver
Carvalho LML, Jorge AA de L, Branco EV, Oliveira DF de, Haddad LA, Bertola DR, Rosenberg C, Krepischi ACV. EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome [Internet]. Molecular Neurobiology. 2025 ; 62 5977–5989.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1007/s12035-024-04655-x - A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis
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Informações sobre o DOI: 10.1007/s12035-024-04655-x (Fonte: oaDOI API)
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