Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation (1999)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; TSANACLIS, ANA MARIA CROUS - FM ; DIAMENT, ARON JUDKA - FM ; LEVY, JOSE ANTONIO - FM
- Unidade: FM
- DOI: 10.1016/s0387-7604(98)00100-4
- Assunto: NEUROLOGIA
- Language: Inglês
- Source:
- Título: Brain & Development
- Volume/Número/Paginação/Ano: v. 21, p. 274-278, 1999
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
REED, Umbertina Conti et al. Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation. Brain & Development, v. 21, p. 274-278, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0387-7604(98)00100-4. Acesso em: 29 dez. 2025. -
APA
Reed, U. C., Tsanaclis, A. M. C., Vainzof, M., Marie, S. K. N., Carvalho, M. S., Rozeinblatt, J., et al. (1999). Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation. Brain & Development, 21, 274-278. doi:10.1016/s0387-7604(98)00100-4 -
NLM
Reed UC, Tsanaclis AMC, Vainzof M, Marie SKN, Carvalho MS, Rozeinblatt J, Pedreira CC, Diament AJ, Levy JA. Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation [Internet]. Brain & Development. 1999 ; 21 274-278.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1016/s0387-7604(98)00100-4 -
Vancouver
Reed UC, Tsanaclis AMC, Vainzof M, Marie SKN, Carvalho MS, Rozeinblatt J, Pedreira CC, Diament AJ, Levy JA. Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation [Internet]. Brain & Development. 1999 ; 21 274-278.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1016/s0387-7604(98)00100-4 - Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement
- Afeccao muscular associada a catarata: relato de dois irmaos
- Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement
- Miopatia centronuclear (miotubular): relato de caso
- Congenital muscular dystrophy: clinical and pathologic review of 24 patients
- Autosomal recessive nondystrophic myotonia
- Congenital structural myopathies: clinical and pathologic review of 13 patients
- Miopatia miotubular: relato de caso
- Congenital muscular dystrophy: clinical and pathologic review of 24 patients
- Congenital structural myopathies: clinical and pathologic review of 13 patients
Informações sobre o DOI: 10.1016/s0387-7604(98)00100-4 (Fonte: oaDOI API)
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