Source: Neuropediatrics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
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: 30 abr. 2024.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 2024 abr. 30 ]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 2024 abr. 30 ]