Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.

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Bibliographic Details
Title: Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
Authors: Elsayed, Solaf M1, Heller, Raoul2, Thoenes, Michaela2, Zaki, Maha S3, Swan, Daniel4, Elsobky, Ezzat1, Zühlke, Christine5, Ebermann, Inga2, Nürnberg, Gudrun6, Nürnberg, Peter6, Bolz, Hanno J7
Source: European Journal of Human Genetics. Feb2014, Vol. 22 Issue 2, p286-288. 3p.
Database: Academic Search Ultimate
Description
ISSN:10184813
DOI:10.1038/ejhg.2013.150