Citations for
1PDE8B, SNID2
A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration.
Azuma R, Ishikawa K, Hirata K, Hashimoto Y, Takahashi M, Ishii K, Inaba A, Yokota T, Orimo S.
Mov Disord 30(14):1964-7. doi: 10.1002/mds.26345. Epub 2015 Oct 13. 2015
2PDE8B, SNID2
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.
Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G.
Am J Hum Genet 86(1):83-7.PMID: 20085714 2010
3SNID2
Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.
Kuhlenbaumer G, Ludemann P, Schirmacher A, De Vriendt E, Hunermund G, Young P, Hund-Georgiadis M, Schuierer G, Moller H, Ringelstein EB, Van Broeckhoven C, Timmerman V, Stogbauer F.
Neurology 62(12):2203-8. 2004