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

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

Bibliographic Details
Main Authors: Synofzik, Matthis, Schüle, Rebecca, Schulze, Martin, Gburek-Augustat, Janina, Schweizer, Roland, Schirmacher, Anja, Krägeloh-Mann, Ingeborg, Gonzalez, Michael, Young, Peter, Züchner, Stephan, Schöls, Ludger, Bauer, Peter
Format: Online
Language:English
Published: BioMed Central 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021831/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021831/

Similar Items