Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts
Work
Year: 2014
Type: article
Abstract: Mutations in the gene STUB1, encoding the protein CHIP (C-terminus of HSC70-interacting protein), have recently been suggested as a cause of recessive ataxia based on the findings in few Chinese famil... more
Authors Matthis Synofzik, Rebecca Schüle, Martin Schulze, Janina Gburek‐Augustat, Roland Schweizer +7 more
Institutions University of Tübingen, Hertie Institute for Clinical Brain Research, University Hospital Münster, University of Miami, Dr. John T. Macdonald Foundation +1 more
Cites: 18
Cited by: 59
Related to: 10
FWCI: 1.772
Citation percentile (by year/subfield): 87.99
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Sustainable Development Goal Good health and well-being
Open Access status: gold
APC paid (est): $1,806