Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations
Elsayed, Solaf M, Heller, Raoul, Thoenes, Michaela, Zaki, Maha S, Swan, Daniel, Elsobky, Ezzat, Zühlke, Christine, Ebermann, Inga, Nürnberg, Gudrun, Nürnberg, Peter, Bolz, Hanno JТом:
22
Мова:
english
Журнал:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2013.150
Date:
February, 2014
Файл:
PDF, 595 KB
english, 2014