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Journal Article
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