Novel TUBB4A mutation in a family with hereditary spastic paraplegia

Acta Neurol Belg. 2023 Aug;123(4):1561-1563. doi: 10.1007/s13760-022-02032-w. Epub 2022 Jul 23.

Authors

Dayao Lv¹, Jinyu Lu¹, Gaohua Zhao¹, Hui Liang², Guohua Zhao³

Affiliations

¹ Department of Neurology, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, China.
² Department of Neurology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. wen1937@S163.com.
³ Department of Neurology, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, China. gzhao@zju.edu.cn.

PMID: 35871212
DOI: 10.1007/s13760-022-02032-w

No abstract available

Keywords: Hypomyelinating leukodystrophy; Mutation; Spastic paralysis; TUBB4A.

Publication types

Letter

MeSH terms

Humans
Mutation / genetics
Pedigree
Spastic Paraplegia, Hereditary* / genetics
Tubulin / genetics

Substances

TUBB4A protein, human
Tubulin