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, cilt.33, sa.3, ss.494-500, 2016 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33 Sayı: 3
  • Basım Tarihi: 2016
  • Dergi Adı: JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.494-500
  • İstanbul Üniversitesi Adresli: Evet

Özet

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