Publication Date:
2013-07-11
Description:
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations European Journal of Human Genetics advance online publication, July 10 2013. doi:10.1038/ejhg.2013.150 Authors: Solaf M Elsayed, Raoul Heller, Michaela Thoenes, Maha S Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg & Hanno J Bolz
Keywords:
SPTBN2spinocerebellar ataxiaSCA5β-III spectrin
Print ISSN:
1018-4813
Electronic ISSN:
1476-5438
Topics:
Biology
,
Medicine
Permalink