Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts

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Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts

Author: Synofzik, Matthis; Schuele, Rebecca; Schulze, Martin; Gburek-Augustat, Janina; Schweizer, Roland; Schirmacher, Anja; Kraegeloh-Mann, Ingeborg; Gonzalez, Michael; Young, Peter; Zuechner, Stephan; Schoels, Ludger; Bauer, Peter
Tübinger Autor(en):
Schulze, Martin
Gburek-Augustat, Janina
Schweizer, Roland
Bauer, Peter
Synofzik, Matthis Benjamin
Schüle-Freyer, Rebecca
Krägeloh-Mann, Ingeborg
Schöls, Ludger
Published in: Orphanet Journal of Rare Diseases (2014), Bd. 9, Article 57
Verlagsangabe: Biomed Central Ltd
Language: English
Full text: http://dx.doi.org/10.1186/1750-1172-9-57
ISSN: 1750-1172
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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