Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia (2007)
Valdmanis, Paul N.; Meijer, Inge A.; Reynolds, Annie; Lei, Adrienne; MacLeod, Patrick; Schlesinger, David; Zatz, Mayana 
; Reid, Evan; Dion, Patrick A.; Drapeau, Pierre; Rouleau, Guy A.
Source: American Journal of Human Genetics. Unidade: IB
Subjects: DOENÇAS NEURODEGENERATIVAS, DOENÇAS HEREDITÁRIAS
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VALDMANIS, Paul N. et al. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics, v. 80, n. 1, p. 152-161, 2007Tradução . . Acesso em: 09 nov. 2024.APA
Valdmanis, P. N., Meijer, I. A., Reynolds, A., Lei, A., MacLeod, P., Schlesinger, D., et al. (2007). Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics, 80( 1), 152-161.NLM
Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics. 2007 ; 80( 1): 152-161.[citado 2024 nov. 09 ]Vancouver
Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics. 2007 ; 80( 1): 152-161.[citado 2024 nov. 09 ]
