SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegia

Authors

Keywords

Hereditary spastic paraparesis, Ataxia, GLUT1, Paroxysmal choreo-atethosis, DYT18, DYT9

Journal

Volume -, Issue -, Pages -

Publisher

Elsevier BV

Online

2018-12-18

DOI

10.1016/j.ejpn.2018.12.004

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