Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination
Viorica Chelban(National Hospital for Neurology and Neurosurgery), Henry Houlden(Queen Mary University of London), Juan A. Botía(University College London), Stéphanie Efthymiou(Queen Mary University of London), Fahad A. Bashiri(King Saud University), Mina Ryten(Guy's Hospital), M. Natalia Zanetti(Epilepsy Research UK), Jana Vandrovcová(Texas Tech University), Nicholas Wood(National Hospital for Neurology and Neurosurgery), Eloise Tribollet(Queen Mary University of London), Oscar D. Bello(Department of Embryology), Fowzan S. Alkuraya(Alfaisal University), Nisha Patel(King Faisal Specialist Hospital & Research Centre), David S. Lynch(University College London), James E. Rothman(Epilepsy Research UK), Indran Davagnanam(University College London)
Cited by 51
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
The transcriptional landscape of age in human peripheral blood
|Nature Communications|2015|774