L-2-Hydroxyglutaric Aciduria: Report of Four Turkish Patients from the Same Family

Date
2016
Author
Yalcin, A. Destina
Tekturk, Pinar
Yapici, Zuhal
Metadata
Show full item record
Abstract
Background: L-2-Hydroxyglutaric aciduria is a rare slow progressive autosomal recessively inherited neurometabolic disease.
URI
http://hdl.handle.net/20.500.12627/89196
Collections