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

Yalcin A. D., Tekturk P., Yapici Z.

JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, vol.33, no.3, pp.494-500, 2016 (SCI-Expanded, Scopus, TRDizin)

  • Publication Type: Article / Article
  • Volume: 33 Issue: 3
  • Publication Date: 2016
  • Journal Name: JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.494-500
  • Istanbul University Affiliated: Yes

Abstract

Background: L-2-Hydroxyglutaric aciduria is a rare slow progressive autosomal recessively inherited neurometabolic disease.