Open AccessNovel SPG4 Mutation in a Patient with Sporadic Hereditary Spastic Paraplegia and Elevated Cerebrospinal Fluid Protein
Author(s) -
Hongda She,
Xin Zheng,
Yingxiu Xiao,
Frank Mastaglia,
P. Anthony Akkari,
Jing-Shan Wu
Publication year - 2021
Publication title -
journal of clinical neurology/the journal of clinical neurology
Language(s) - English
Resource type - Journals
eISSN - 2005-5013
pISSN - 1738-6586
DOI - 10.3988/jcn.2021.17.1.152
Subject(s) - hereditary spastic paraplegia , medicine , mutation , cerebrospinal fluid , paraplegia , spastic , pathology , genetics , phenotype , biology , gene , physical therapy , spinal cord , cerebral palsy , psychiatry