Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene (2011)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; CHADI, GERSON - FM
- Unidade: FM
- DOI: 10.1016/j.nmd.2011.06.831
- Subjects: DISTROFIA MUSCULAR; DOENÇAS NEURODEGENERATIVAS; MUTAÇÃO GENÉTICA; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 21, n. 9-10, p. 663, res. P2.8, 2011
- Conference titles: International Congress of the World Muscle Society
- Status:
- Nenhuma versão em acesso aberto identificada
-
ABNT
PASQUALIN, L. M. et al. Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.831. Acesso em: 18 mar. 2026. , 2011 -
APA
Pasqualin, L. M., Zanoteli, E., Albuquerque, M. A. V., Martins, C. A., Neto, O. L. A., Resende, M. B. D., et al. (2011). Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.831 -
NLM
Pasqualin LM, Zanoteli E, Albuquerque MAV, Martins CA, Neto OLA, Resende MBD, Chadi G, Reed UC. Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 663.[citado 2026 mar. 18 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.831 -
Vancouver
Pasqualin LM, Zanoteli E, Albuquerque MAV, Martins CA, Neto OLA, Resende MBD, Chadi G, Reed UC. Congenital muscular dystrophy with intracytoplasmatic aggregates on muscle biopsy caused by mutation on LMNA gene [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 663.[citado 2026 mar. 18 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.831 - Multiplex PCR for identifying DMD gene deletions in children with Duchenne/Becker muscular dystrophy (DMD/BMD)
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