Rocco, P S; Vainzof, Mariz 
; Froehner, S C; Marie, Suely Kazue Nagahashi; Kunkel, Louis M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: American Society of Human Genetics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
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ABNT
ROCCO, P S et al. Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 nov. 2024. , 1999APA
Rocco, P. S., Vainzof, M., Froehner, S. C., Marie, S. K. N., Kunkel, L. M., Passos-Bueno, M. R., & Zatz, M. (1999). Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.NLM
Rocco PS, Vainzof M, Froehner SC, Marie SKN, Kunkel LM, Passos-Bueno MR, Zatz M. Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 nov. 19 ]Vancouver
Rocco PS, Vainzof M, Froehner SC, Marie SKN, Kunkel LM, Passos-Bueno MR, Zatz M. Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 nov. 19 ]
