A 7-year-old Boy with Hand Tremors and a Novel Mutation for L-2-hydroxyglutaric Aciduria.

Olgac, A; Tekin, Orgun L; Ezgü, F S; BiberoÇ§lu, G; Tümer, L

Olgac, A; Tekin, Orgun L; Ezgü, F S; BiberoÇ§lu, G; Tümer, L.

Afiliación

Olgac A; Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
Tekin OL; Department of Pediatric Neurology, Gazi University Hospital, Ankara, Turkey.
Ezgü FS; Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
BiberoÇ§lu G; Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
Tümer L; Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.

Balkan J Med Genet ; 22(2): 93-96, 2019 Dec.

Article en En | MEDLINE | ID: mdl-31942424

Palabras clave

Inborn errors of metabolism; L-2-hydroxyglutaric aciduria (L2HGA); Seizure; Tremor

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Balkan J Med Genet Año: 2019 Tipo del documento: Article País de afiliación: Turquía

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