Source: Brain & Development. Unidades: FM, IB
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
ABNT
REED, Umbertina Conti et al. Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency. Brain & Development, v. 18, p. 53-8, 1996Tradução . . Disponível em: https://doi.org/10.1016/0387-7604(95)00095-x. Acesso em: 19 ago. 2024.APA
Reed, U. C., Marie, S. K. N., Vainzof, M., Salum, P. B., Levy, J. A., Zatz, M., & Diament, A. J. (1996). Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency. Brain & Development, 18, 53-8. doi:10.1016/0387-7604(95)00095-xNLM
Reed UC, Marie SKN, Vainzof M, Salum PB, Levy JA, Zatz M, Diament AJ. Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency [Internet]. Brain & Development. 1996 ;18 53-8.[citado 2024 ago. 19 ] Available from: https://doi.org/10.1016/0387-7604(95)00095-xVancouver
Reed UC, Marie SKN, Vainzof M, Salum PB, Levy JA, Zatz M, Diament AJ. Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency [Internet]. Brain & Development. 1996 ;18 53-8.[citado 2024 ago. 19 ] Available from: https://doi.org/10.1016/0387-7604(95)00095-x