OMIM/604277[Secondary Source ID] - Search Results

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Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.

Eymard-Pierre E, Lesca G, Dollet S, Santorelli FM, di Capua M, Bertini E, Boespflug-Tanguy O. Eymard-Pierre E, et al. Am J Hum Genet. 2002 Sep;71(3):518-27. doi: 10.1086/342359. Epub 2002 Jul 26. Am J Hum Genet. 2002. PMID: 12145748 Free PMC article.

Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene.

Chinnery PF, Keers SM, Holden MJ, Ramesh V, Dalton A. Chinnery PF, et al. Neurology. 2004 Aug 24;63(4):710-2. doi: 10.1212/01.wnl.0000135346.63675.3e. Neurology. 2004. PMID: 15326248

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