A novel KIAA0196 (SPG8) mutation in a Chinese family with spastic paraplegia
Chin Med J (Engl)
.
2014;127(10):1987-9.
Authors
Xianling Wang
1
,
Yanhui Yang
2
,
Xiangbo Wang
1
,
Cunjiang Li
3
,
Jianping Jia
1
Affiliations
1
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China.
2
Department of Radiology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China.
3
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China. Email: lcj818@sina.com.
PMID:
24824269
No abstract available
MeSH terms
Adolescent
Adult
Female
Humans
Mutation
Paraplegia / genetics*
Polymerase Chain Reaction
Proteins / genetics*
Young Adult
Substances
Proteins
WASHC5 protein, human