STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations
Hayer, Stefanie Nicole, Deconinck, Tine, Bender, Benjamin, Smets, Katrien, Züchner, Stephan, Reich, Selina, Schöls, Ludger, Schüle, Rebecca, De Jonghe, Peter, Baets, Jonathan, Synofzik, MatthisVolume:
12
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-017-0580-x
Date:
December, 2017
File:
PDF, 1.45 MB
english, 2017