L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine.
Roberto Leal-OrtegaLuis Enrique Parra-MedinaLizbeth Josefina González-HerreraPublished in: Tremor and other hyperkinetic movements (New York, N.Y.) (2024)
gene, and improvement of symptoms with vitamin supplements and levocarnitine.