Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations (2014)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1016/j.pediatrneurol.2014.01.036
- Subjects: DISTROFIA MUSCULAR; MUTAÇÃO GENÉTICA; MÚSCULO ESQUELÉTICO (ANORMALIDADES)
- Language: Inglês
- Imprenta:
- Publisher place: Chippewa Falls (US)
- Date published: 2014
- Source:
- Título: Pediatric Neurology
- ISSN: 0887-8994
- Volume/Número/Paginação/Ano: v. 50, n. 5, p. e11-e12, 2014
- Status:
- Artigo possui versão em acesso aberto em repositório (Green Open Access)
- Versão do Documento:
- Versão submetida (Pré-print)
- Acessar versão aberta:
-
ABNT
ALBUQUERQUE, Marco A. V. et al. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations. Pediatric Neurology, v. 50, n. 5, p. e11-e12, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2014.01.036. Acesso em: 15 abr. 2026. -
APA
Albuquerque, M. A. V., Pasqualin, L. M., Martins, C. A., Reed, U. C., & Zanoteli, E. (2014). Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations. Pediatric Neurology, 50( 5), e11-e12. doi:10.1016/j.pediatrneurol.2014.01.036 -
NLM
Albuquerque MAV, Pasqualin LM, Martins CA, Reed UC, Zanoteli E. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations [Internet]. Pediatric Neurology. 2014 ; 50( 5): e11-e12.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2014.01.036 -
Vancouver
Albuquerque MAV, Pasqualin LM, Martins CA, Reed UC, Zanoteli E. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations [Internet]. Pediatric Neurology. 2014 ; 50( 5): e11-e12.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2014.01.036 - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
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