Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation (2023)
- Authors:
- USP affiliated authors: LUCATO, LEANDRO TAVARES - FM ; REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM ; CAMELO, CLARA GONTIJO - FM
- Unidade: FM
- DOI: 10.3233/JND-221638
- Subjects: DISTROFIA MUSCULAR; MALFORMAÇÕES; CÉREBRO; VARIAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of neuromuscular diseases
- ISSN: 2214-3599
- Volume/Número/Paginação/Ano: v. 10, n. 4, p. 483-492, 2023
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: unspecified-oa
-
ABNT
CAMELO, Clara Gontijo et al. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation. Journal of neuromuscular diseases, v. 10, n. 4, p. 483-492, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/56122. Acesso em: 30 dez. 2025. -
APA
Camelo, C. G., Artilheiro, M. C., Moreno, C. A. M., Ferraciolli, S. F., Silva, A. M. S. da, Fernandes, T. R., et al. (2023). Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation. Journal of neuromuscular diseases, 10( 4), 483-492. doi:10.3233/JND-221638 -
NLM
Camelo CG, Artilheiro MC, Moreno CAM, Ferraciolli SF, Silva AMS da, Fernandes TR, Lucato LT, Rocha AJ, Reed UC, Zanoteli E. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation [Internet]. Journal of neuromuscular diseases. 2023 ; 10( 4): 483-492.[citado 2025 dez. 30 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56122 -
Vancouver
Camelo CG, Artilheiro MC, Moreno CAM, Ferraciolli SF, Silva AMS da, Fernandes TR, Lucato LT, Rocha AJ, Reed UC, Zanoteli E. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation [Internet]. Journal of neuromuscular diseases. 2023 ; 10( 4): 483-492.[citado 2025 dez. 30 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56122 - A novel acta 1 mutation in a patient with nemaline myopathy
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Informações sobre o DOI: 10.3233/JND-221638 (Fonte: oaDOI API)
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