Severe 5,10‐methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia

Publisher： John Wiley & Sons Inc

E-ISSN： 1468-1331|25|3|602-605

ISSN： 1351-5101

Source： EUROPEAN JOURNAL OF NEUROLOGY, Vol.25, Iss.3, 2018-03, pp. : 602-605

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