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Publication : Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.

First Author  Hanein S Year  2008
Journal  Am J Hum Genet Volume  82
Issue  4 Pages  992-1002
PubMed ID  18394578 Mgi Id 
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