A novel missense mutation confirms ATL3 as a gene for hereditary sensory neuropathy type 1.
作者信息
Fischer Dirk, Schabhüttl Maria, Wieland Thomas, Windhager Reinhard, Strom Tim M, Auer-Grumbach Michaela
机构信息
1 Department of Neurology, University of Basel Hospital, 4031 Basel, Switzerland2 Division of Neuropaediatrics, University of Basel Childrens Hospital, 4056 Basel, Switzerland.
3 Department of Orthopaedics, Medical University Vienna, 1090 Vienna, Austria.
出版信息
Brain. 2014 Jul;137(Pt 7):e286. doi: 10.1093/brain/awu091. Epub 2014 Apr 15.
PMID:24736309
Abstract
摘要
Zotero 插件