SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission
James Fasham(University of Exeter), Christian A. Hübner(University of Wuppertal), Joseph G. Gleeson(Howard Hughes Medical Institute), Maha S. Zaki(National Research Centre), Saskia B. Wortmann(Paracelsus Medical University), Nishanka Ubeyratna(University of Exeter), Peter D. Turnpenny(University of Exeter), Kai Kaila(University of Helsinki), Matthew N. Wakeling(University of Exeter), Andrew H. Crosby(University of Exeter), Reham Khalaf‐Nazzal(Arab American University), Imad Dweikat(Arab American University), Martina Wilke(Erasmus MC), Marjon van Slegtenhorst(Erasmus MC), Nderim Kryeziu(Jena University Hospital), Bassam Abu‐Libdeh(Al-Quds University), Hanan E. Shamseldin(King Faisal Specialist Hospital & Research Centre), Joseph S. Leslie(University of Exeter), Henry Houlden(University College London), Lutz Liebmann(Jena University Hospital), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Fowzan S. Alkuraya(Alfaisal University), Peter Schlattmann(Kliniken Maria Hilf), Emma L. Baple(University of Exeter), Lucy McGavin(University Hospitals Plymouth NHS Trust), Antje K. Huebner(Jena University Hospital), Muhannad Daana, Grazia M.S. Mancini(Erasmus MC), Mohamed Almuhaizea(King Faisal Specialist Hospital & Research Centre), Tobias B. Haack(Technical University of Munich)
Cited by 18
Related Papers
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
The global burden of paediatric and neonatal sepsis: a systematic review
|The Lancet Respiratory Medicine|2018|1.1k
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
|Nature Genetics|2012|752
Phase Synchrony among Neuronal Oscillations in the Human Cortex
|Journal of Neuroscience|2005|681