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Neurogenetics|December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosisE Seboun, J R Oksenberg, A Rombos, et al.Neurogenetics|December 14, 1999
The human glia maturation factor-gamma gene: genomic structure and mutation analysis in gliomas with chromosome 19q lossN Peters, J S Smith, I Tachibana, et al.Neurogenetics|December 14, 1999
Potential treatment of transthyretin-type amyloidoses by sulfiteK Altland, P WinterNeurogenetics|September 13, 2000
Parkinson disease: analysis of mitochondrial DNA in monozygotic twinsS Kösel, E M Grasbon-Frodl, J M Hagenah, et al.Neurogenetics|November 14, 2017
ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variationJing-Yang Wang, Peng Zhou, Jie Wang, et al.Neurogenetics|December 20, 2018
Sudden unexpected death with rare compound heterozygous variants in PRICKLE1Yukiko Hata, Koji Yoshida, Naoki NishidaNeurogenetics|December 7, 2017
Clinical application of next generation sequencing in hereditary spinocerebellar ataxia: increasing the diagnostic yield and broadening the ataxia-spasticity spectrum. A retrospective analysisDaniele Galatolo, Alessandra Tessa, Alessandro Filla, et al.Neurogenetics|December 14, 2019
Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2Shan Lin, Liu-Qing Xu, Guo-Rong Xu, et al.Neurogenetics|March 18, 2018
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS)C Ranieri, S Di Tommaso, D C Loconte, et al.Neurogenetics|August 29, 2001
Hereditary neuralgic amyotrophyJ Meuleman, V Timmerman, C Van Broeckhoven, et al.Pageof 96