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Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A.

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第一作者: Akane,Terasaki
第一单位: Department of Psychiatry, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
作者单位: Department of Psychiatry, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan. [1] Department of Psychiatry, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan. nakamu36@m.kufm.kagoshima-u.ac.jp. [2] Department of Neurology, Kurashiki-kinen Hospital, Kurashiki, Japan. [3] Musashinokokubunji Clinic, Tokyo, Japan. [4] Department of Comprehensive Rehabilitation Science, Hirosaki University Graduate School of Health Sciences, Hirosaki, Japan. [5] North Tohoku Epilepsy Center, Minato Hospital, Aomori, Japan.;Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan. [6] Department of Neuropsychiatry, Fukushima Medical University School of Medicine, Fukushima, Japan. [7] Department of Psychiatry, Aizu Medical Center, Fukushima Medical University, Fukushima, Japan. [8] Hashimoto Clinic, Tokyo, Japan. [9] Department of Neurology, Amagasaki Daimotsu Hospital, Amagasaki, Japan. [10] Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.;Medical Genome Center, National Center of Neurology and Psychiatry, Tokyo, Japan. [11] Department of Neurology, Kindai University Faculty of Medicine, Osaka, Japan. [12] Department of Neurology, Suita Municipal Hospital, Osaka, Japan. [13] Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan. [14]
DOI 10.1038/s10038-020-00867-w
PMID 33184460
发布时间 2021-03-25
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Journal of human genetics

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