 | Up a level |
2014
Doss, Sarah, Lohmann, Katja, Seibler, Philip, Arns, Bjoern, Klopstock, Thomas, Zuehlke, Christine, Freimann, Karen, Winkler, Susen, Lohnau, Thora, Drungowski, Mario, Nuernberg, Peter, Wiegers, Karin, Lohmann, Ebba, Naz, Sadaf 
ORCID: 0000-0002-1912-0235, Kasten, Meike, Bohner, Georg ORCID: 0000-0002-1919-092X, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Endres, Matthias and Klein, Christine
(2014).
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.
J. Neurol., 261 (1).
S. 207 - 213.
HEIDELBERG:
SPRINGER HEIDELBERG.
ISSN 1432-1459
Elsayed, Solaf M., Heller, Raoul, Thoenes, Michaela, Zaki, Maha S., Swan, Daniel ORCID: 0000-0001-8978-8129, Elsobky, Ezzat, Zuehlke, Christine, Ebermann, Inga, Nuernberg, Gudrun, Nuernberg, Peter and Bolz, Hanno J.
(2014).
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
Eur. J. Hum. Genet., 22 (2).
S. 286 - 289.
LONDON:
NATURE PUBLISHING GROUP.
ISSN 1476-5438