Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations (1995)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; REED, UMBERTINA CONTI - FM ; ZATZ, MAYANA - IB
- Unidades: IB; FM
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Source:
- Título: Neuropediatrics
- Volume/Número/Paginação/Ano: v.26, p.293-7, 1995
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ABNT
VAINZOF, Mariz et al. Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics, v. 26, p. 293-7, 1995Tradução . . Acesso em: 29 dez. 2025. -
APA
Vainzof, M., Marie, S. K. N., Reed, U. C., Schwartzman, J. S., Pavanello, R. C. M., Passos-Bueno, M. R., & Zatz, M. (1995). Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics, 26, 293-7. -
NLM
Vainzof M, Marie SKN, Reed UC, Schwartzman JS, Pavanello RCM, Passos-Bueno MR, Zatz M. Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics. 1995 ;26 293-7.[citado 2025 dez. 29 ] -
Vancouver
Vainzof M, Marie SKN, Reed UC, Schwartzman JS, Pavanello RCM, Passos-Bueno MR, Zatz M. Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics. 1995 ;26 293-7.[citado 2025 dez. 29 ] - Molecular analysis of spinal muscular atrophy in brazilian patients
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