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WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study
Authors:J.‐H. Yuan  A. Hashiguchi  A. Yoshimura  N. Sakai  M.P. Takahashi  T. Ueda  A. Taniguchi  S. Okamoto  N. Kanazawa  Y. Yamamoto  K. Saigoh  S. Kusunoki  M. Ando  Y. Hiramatsu  Y. Okamoto  H. Takashima
Affiliation:1. Department of Neurology and Geriatrics, Kagoshima University, Graduate School of Medical and Dental Sciences, Kagoshima, Japan;2. Child Healthcare and Genetic Science Laboratory, Division of Health Science, Osaka University, Graduate School of Medicine, Osaka, Japan;3. Department of Functional Diagnostic Science, Division of Health Science, Osaka University, Graduate School of Medicine, Osaka, Japan;4. Division of Neurology, Kobe University, Graduate School of Medicine, Kobe, Japan;5. Department of Neurology, Mie University, Graduate School of Medicine, Mie, Japan;6. Department of Rehabilitation Medicine, Fujita Health University, Nanakuri Memorial Hospital, Mie, Japan;7. Department of Dermatology, Wakayama Medical University, Wakayama, Japan;8. Department of Neurology, Kindai University, Faculty of Medicine, Osaka, Japan
Abstract:
Keywords:founder mutation  hereditary sensory and autonomic neuropathy  next‐generation sequencing  WNK1/HSN2
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