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 do periódico: Pediatric Neurology
- ISSN: 0887-8994
- Volume/Número/Paginação/Ano: v. 50, n. 5, p. e11-e12, 2014
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ALBUQUERQUE, Marco A. V.; PASQUALIN, Lívia M.; MARTINS, Cristiane A.; REED, Umbertina C.; ZANOTELI, Edmar. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations. Pediatric Neurology, Chippewa Falls (US), v. 50, n. 5, p. e11-e12, 2014. Disponível em: < http://dx.doi.org/10.1016/j.pediatrneurol.2014.01.036 > DOI: 10.1016/j.pediatrneurol.2014.01.036. -
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.Available from: http://dx.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.Available from: http://dx.doi.org/10.1016/j.pediatrneurol.2014.01.036 - Atypical phenotype in a case of MYH7 congenital myopathy
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Informações sobre o DOI: 10.1016/j.pediatrneurol.2014.01.036 (Fonte: oaDOI API)
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