Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum

Published 2008 View Full Article

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Title
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
Authors
Keywords
-
Journal
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 79, Issue 5, Pages 607-609
Publisher
BMJ
Online
2008-04-14
DOI
10.1136/jnnp.2007.136390

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