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Molecular Genetics & Genomic Medicine
(May 2022)
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
Qiao Wei,
Pei‐Shan Wang,
Hai‐Lin Dong,
Wen‐Jiao Luo,
Zhi‐Ying Wu,
Hong‐Fu Li
Affiliations
Qiao Wei
Department of Neurology and Research Center of Neurology Second Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
Pei‐Shan Wang
Department of Neurology and Research Center of Neurology Second Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
Hai‐Lin Dong
Department of Neurology and Research Center of Neurology Second Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
Wen‐Jiao Luo
Department of Neurology and Research Center of Neurology Second Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
Zhi‐Ying Wu
Department of Neurology and Research Center of Neurology Second Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
Hong‐Fu Li
Department of Neurology and Research Center of Neurology Second Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
DOI
https://doi.org/10.1002/mgg3.1927
Journal volume & issue
Vol. 10, no. 5
pp. n/a – n/a
Abstract
Read online
No abstracts available.
Keywords
Chinese
hereditary spastic paraplegias
UBAP1
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