Mini Review
Published on 22 Feb 2019
Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle Metabolism
in Movement Disorders
Frontiers in Neurology
doi 10.3389/fneur.2019.00131
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- 33 citations
