Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination (2023)
- Authors:
- USP affiliated authors: MONTENEGRO, LUCIANA RIBEIRO - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- DOI: 10.1210/clinem/dgad151
- Subjects: MUTAÇÃO GENÉTICA; PUBERDADE PRECOCE; WESTERN BLOTTING; CRIANÇAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2023
- Source:
- Título do periódico: Journal of clinical endocrinology & metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 108, n. 7, p. 1646-1656, 2023
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
MAGNOTTO, John C et al. Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination. Journal of clinical endocrinology & metabolism, v. 108, n. 7, p. 1646-1656, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54585. Acesso em: 29 maio 2024. -
APA
Magnotto, J. C., Mancini, A., Bird, K., Montenegro, L., Tutunculer, F., Pereira, S. A., et al. (2023). Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination. Journal of clinical endocrinology & metabolism, 108( 7), 1646-1656. doi:10.1210/clinem/dgad151 -
NLM
Magnotto JC, Mancini A, Bird K, Montenegro L, Tutunculer F, Pereira SA, Simas V, Garcia L, Roberts SA, Xavier ACL. Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 7): 1646-1656.[citado 2024 maio 29 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54585 -
Vancouver
Magnotto JC, Mancini A, Bird K, Montenegro L, Tutunculer F, Pereira SA, Simas V, Garcia L, Roberts SA, Xavier ACL. Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 7): 1646-1656.[citado 2024 maio 29 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54585 - Pathogenic variants inTNRC6Bcause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
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Informações sobre o DOI: 10.1210/clinem/dgad151 (Fonte: oaDOI API)
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