171. Characterization of a KCNB1 variant associated with autism, intellectual disability, and epilepsy. (December 2017) Authors: Calhoun, Jeffrey D.; Vanoye, Carlos G.; Kok, Fernando; George, Alfred L.; Kearney, Jennifer A. Journal: Neurology Issue: Volume 3:Number 6(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
172. Characterization of a novel stimulus-induced glial calcium wave in Drosophila larval peripheral segmental nerves and its role in PKG-modulated thermoprotection. (3rd July 2021) Authors: Krill, Jennifer L.; Dawson-Scully, Ken Journal: Journal of neurogenetics Issue: Volume 35:Number 3(2021) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
173. Characterization of axonal transport defects in Drosophila Huntingtin mutants. (1st October 2016) Authors: Weiss, Kurt R.; Littleton, J. Troy Journal: Journal of neurogenetics Issue: Volume 31:Number 1/2(2017) Page Start: 212 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
174. Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34. (April 2020) Authors: Beaudin, Marie; Sellami, Leila; Martel, Christian; Touzel-Deschênes, Lydia; Houle, Gabrielle; Martineau, Laurence; Lacroix, Kevin; Lavallée, Andréane; Chrestian, Nicolas; Rouleau, Guy A.; Gros-Louis, François; Laforce, Robert; Dupré, Nicolas Journal: Neurology Issue: Volume 6:Number 2(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
175. CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease. (June 2015) Authors: Auranen, Mari; Ylikallio, Emil; Shcherbii, Maria; Paetau, Anders; Kiuru-Enari, Sari; Toppila, Jussi P.; Tyynismaa, Henna Journal: Neurology Issue: Volume 1:Number 1(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
176. Child Harold. (3rd July 2018) Authors: Atwood, Margaret Journal: Journal of neurogenetics Issue: Volume 32:Number 3(2018) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
177. Child Harold. (3rd July 2018) Authors: Sokolowski, Marla B Journal: Journal of neurogenetics Issue: Volume 32:Number 3(2018) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
178. Childhood-onset epileptic encephalopathy due to FGF12 exon 1–4 tandem duplication. (October 2020) Authors: Verheyen, Sarah; Speicher, Michael R.; Ramler, Barbara; Plecko, Barbara Journal: Neurology Issue: Volume 6:Number 5(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
179. Children with 5′-end NF1 gene mutations are more likely to have glioma. (October 2017) Authors: Anastasaki, Corina; Morris, Stephanie M.; Gao, Feng; Gutmann, David H. Journal: Neurology Issue: Volume 3:Number 5(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
180. Chorea-acanthocytosis: Homozygous 1-kb deletion in VPS13A detected by whole-genome sequencing. (June 2018) Authors: Walker, Susan; Dad, Rubina; Thiruvahindrapuram, Bhooma; Ullah, Muhammed Ikram; Ahmad, Arsalan; Hassan, Muhammad Jawad; Scherer, Stephen W.; Minassian, Berge A. Journal: Neurology Issue: Volume 4:Number 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗