A rare double diagnosis identified via exome sequencing in a patient with complex cerebellar ataxia: a case report.
作者信息
Thomas Quentin, Vitobello Antonio, Fromont Agnès, Philippe Christophe, Thauvin-Robinet Christel
机构信息
Inserm UMR1231 Team GAD, University of Burgundy and Franche-Comté, 21000, Dijon, Besançon, France.
Genetics Center, FHU-TRANSLAD, Dijon Bourgogne University Hospital, 21000, Dijon, France.
出版信息
Neurol Sci. 2023 May;44(5):1795-1797. doi: 10.1007/s10072-022-06546-2. Epub 2023 Jan 6.
PMID:36604382
Abstract
摘要
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