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
doi 10.3389/fneur.2019.00131
- 6,436 views
- 25 citations
