Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese

Author:

Dong Yue,Li Xu-Ying,Wang Xian-Ling,Xu Fanxi,Wang Zhan-Jun,Song Yang,Li Qibin,Lin Ruichai,Wang Chaodong

Publisher

Elsevier BV

Subject

General Neuroscience

Reference30 articles.

1. P. Hedera, Hereditary Spastic Paraplegia Overview. In: M.P. Adam, H.H. Ardinger, R.A. Pagon, S.E. Wallace, L.J.H. Bean, K. Stephens, A. Amemiya (Eds.), GeneReviews(®), University of Washington, Seattle Copyright © 1993-2020, University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle. All rights reserved., Seattle (WA), 1993.

2. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance;Finsterer;J. Neurol. Sci.,2012

3. Clinical features and management of hereditary spastic paraplegia;Faber;Arq. Neuropsiquiatr.,2014

4. Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia;Wei;Transl. neurodegener.,2019

5. A. Noreau, P.A. Dion, G.A. Rouleau, Molecular aspects of hereditary spastic paraplegia, Exp. Cell Res. 325 (2014) 18–26. https://doi.org/ 10.1016/j.yexcr.2014.02.021.

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