Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy
Emer O’Connor(University College London), Nicholas Wood(National Hospital for Neurology and Neurosurgery), Michael G. Hanna(National Hospital for Neurology and Neurosurgery), Silvia Marino(Queen Mary University of London), Viorica Chelban(National Hospital for Neurology and Neurosurgery), Alan Pittman(St George's, University of London), Indran Davagnanam(University College London), Mark Roberts, Stéphanie Efthymiou(Queen Mary University of London), Jana Vandrovcová(Texas Tech University), Andreea Manole(National Hospital for Neurology and Neurosurgery), Henry Houlden(Queen Mary University of London), Enrico Bugiardini, Emma Matthews(St George’s University Hospitals NHS Foundation Trust), Sarah Wiethoff(University College London), Adnan Y. Manzur(Great Ormond Street Hospital), David S. Lynch(University College London)
Cited by 26
Related Papers
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
Ensembl 2012
|Nucleic Acids Research|2011|839
Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences
|Briefings in Bioinformatics|2016|815
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
|Nature Genetics|2011|635