Nesprin-2 (SYNE2) gene mutation causing an Emery-Dreifuss muscular dystrophy phenotype (2014)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- Subjects: DISTROFIA MUSCULAR; FENÓTIPOS; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Arquivos de Neuro-Psiquiatria
- ISSN: 0004-282X
- Volume/Número/Paginação/Ano: v. 72, supl. 2, p. 96, res. P-229, 2014
- Conference titles: Congresso Brasileiro de Neurologia
-
ABNT
ABATH NETO, O. et al. Nesprin-2 (SYNE2) gene mutation causing an Emery-Dreifuss muscular dystrophy phenotype. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2014 -
APA
Abath Neto, O., Estephan, E., Martins, C. A., Reed, U. C., Oliveira, A. S. B., Laporte, J., & Zanoteli, E. (2014). Nesprin-2 (SYNE2) gene mutation causing an Emery-Dreifuss muscular dystrophy phenotype. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Abath Neto O, Estephan E, Martins CA, Reed UC, Oliveira ASB, Laporte J, Zanoteli E. Nesprin-2 (SYNE2) gene mutation causing an Emery-Dreifuss muscular dystrophy phenotype. Arquivos de Neuro-Psiquiatria. 2014 ; 72 96.[citado 2024 abr. 27 ] -
Vancouver
Abath Neto O, Estephan E, Martins CA, Reed UC, Oliveira ASB, Laporte J, Zanoteli E. Nesprin-2 (SYNE2) gene mutation causing an Emery-Dreifuss muscular dystrophy phenotype. Arquivos de Neuro-Psiquiatria. 2014 ; 72 96.[citado 2024 abr. 27 ] - Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
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