Glutaric acidemia type II patient with thalassemia minor and novel electron transfer flavoprotein-A gene mutations: A case report and review of literature

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Saral N. Y., Aksungar F. B., Aktuglu-Zeybek C., Coskun J., Demirelce O., Serteser M.

World Journal of Clinical Cases, cilt.6, sa.14, ss.786-790, 2018 (SCI-Expanded)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 6 Sayı: 14
  • Basım Tarihi: 2018
  • Doi Numarası: 10.12998/wjcc.v6.i14.786
  • Dergi Adı: World Journal of Clinical Cases
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
  • Sayfa Sayıları: ss.786-790
  • Anahtar Kelimeler: Electron transfer flavoprotein-A mutation, Newborn screening, Glutaric acidemia type II, Inborn error of metabolism, Ketone bodies, Case report, ACIDURIA TYPE-II, DEHYDROGENASE-DEFICIENCY
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Evet