HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-021-01649-7.pdf
Reference29 articles.
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2. Mathewson MA, Lieber RL (2015) Pathophysiology of muscle contractures in cerebral palsy. Phys Med RehabilClin N Am 26(1):57–67. https://doi.org/10.1016/j.pmr.2014.09.005
3. de Souza PVS, de Rezende Pinto WBV, de RezendeBatistella GN, Bortholin T, Oliveira ASB (2017) Hereditary spastic paraplegia: clinical and genetic hallmarks. Cerebellum 16(2):525–551. https://doi.org/10.1007/s12311-016-0803-z
4. Klebe S, Stevanin G, Depienne C (2015) Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still counting. Rev Neurol (Paris) 171(6–7):505–530. https://doi.org/10.1016/j.neurol.2015.02.017
5. Schüle R, Wiethoff S, Martus P, Karle KN, Otto S, Klebe S et al (2016) Hereditary spastic paraplegia: clinicogenetic lessons from 608 patients. Ann Neurol 79(4):646–658. https://doi.org/10.1002/ana.24611
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