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

✍ Scribed by T. Pippucci; 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

Book ID: 111065710
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 256 KB
Volume: 16
Category: Article
ISSN: 1351-5101
DOI: 10.1111/j.1468-1331.2008.02367.x

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