Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity.

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Published in Eur J Neurol on January 01, 2009

Authors

T Pippucci1, E Panza, E Pompilii, V Donadio, A Borreca, C Babalini, C Patrono, R Zuntini, T Kawarai, G Bernardi, R Liguori, G Romeo, P Montagna, A Orlacchio, M Seri

Author Affiliations

1: Laboratorio di Genetica Medica, Dipartimento di Scienze Ginecologiche, Ostetriche e Pediatriche, Policlinico Sant'Orsola Malpighi, Università di Bologna, Bologna, Italy. tommaso.pippucci@unibo.it

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