Reply: A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
作者信息
Ylikallio Emil, Woldegebriel Rosa, Tyynismaa Henna
机构信息
Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
Clinical Neurosciences, Neurology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
出版信息
Brain. 2018 Sep 1;141(9):e67. doi: 10.1093/brain/awy185.
PMID:29982292
Abstract
摘要
Zotero 插件