DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Hanein S, Martin E, Boukhris A , et al.
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.
Am J Hum Genet 2008;
82 (4) 992-1002
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