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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
Emanuele Panza, Diego Martinelli, Pamela Magini and 2 more
Frontiers in Neurology · 2019
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Cited by papers we hold 1
- The Janus-like role of proline metabolism in cancer · 2020No notice
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