Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.

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Published in Eur J Neurol on July 01, 2007

Authors

A K Erichsen1, E Inderhaug, M Mattingsdal, K Eiklid, C M E Tallaksen

Author Affiliations

1: Department of Neurology, Ullevål University Hospital, Oslo, Norway. anhs@uus.no

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