HDAC6 Inhibitors Rescued the Defective Axonal Mitochondrial Movement in Motor Neurons Derived from the Induced Pluripotent Stem Cells of Peripheral Neuropathy Patients with <i>HSPB1</i> MutationJi Yon Kim, Byung‐Ok Choi|Stem Cells International|2016Cited by 55
Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1AFeifei Tao, Stephan Züchner, Callyn A. Kirk et al.|Annals of Neurology|2019Cited by 45
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association StudyFeifei Tao, Stephan Züchner, Gary W. Beecham et al.|Journal of Neuromuscular Diseases|2019Cited by 28
Application of whole‐exome sequencing for detecting copy number variants in CMT1A/HNPPHyun Youn Jo, S.K. Koo, M.‐H. Park et al.|Clinical Genetics|2015Cited by 13
Adult onset EBV-associated hemophagocytic lymphohistiocyotosis initially presenting as progressive myelopathy (P6.192)Young Hee Jung, Byoung Joon Kim, Jin Myoung Seok et al.|Neurology|2017Cited by 0