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Page 1
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia.
Ozes B, Karagoz N, Schüle R, Rebelo A, Sobrido MJ, Harmuth F, Synofzik M, Pascual SIP, Colak M, Ciftci-Kavaklioglu B, Kara B, Ordóñez-Ugalde A, Quintáns B, Gonzalez MA, Soysal A, Zuchner S, Battaloglu E. Ozes B, et al. Among authors: pascual sip. Clin Genet. 2017 Nov;92(5):534-539. doi: 10.1111/cge.13008. Epub 2017 Apr 19. Clin Genet. 2017. PMID: 28295203 Free PMC article.
[Congenital vascular malformations in childhood].
Pascual Pascual-Castroviejo I, Viaño J, Pascual SI, Martínez V. Pascual Pascual-Castroviejo I, et al. Rev Neurol. 1999 Aug 1-15;29(3):217-30. Rev Neurol. 1999. PMID: 10797904 Review. Spanish.