STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations

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STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations

Author: Hayer, Stefanie Nicole; Deconinck, Tine; Bender, Benjamin; Smets, Katrien; Zuechner, Stephan; Reich, Selina; Schoels, Ludger; Schuele, Rebecca; De Jonghe, Peter; Baets, Jonathan; Synofzik, Matthis
Tübinger Autor(en):
Bender, Benjamin
Reich, Selina
Synofzik, Matthis Benjamin
Hayer, Stefanie N.
Schöls, Ludger
Schüle-Freyer, Rebecca
Published in: Orphanet Journal of Rare Diseases (2017), Bd. 12, Article 31
Verlagsangabe: Biomed Central Ltd
Language: English
Full text: http://dx.doi.org/10.1186/s13023-017-0580-x
ISSN: 1750-1172
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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