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Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures

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اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • بيانات النشر:
      Korean Child Neurology Society, 2024.
    • الموضوع:
      2024
    • Collection:
      LCC:Internal medicine
      LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
      LCC:Neurology. Diseases of the nervous system
    • File Description:
      electronic resource
    • ISSN:
      2635-909X
      2635-9103
    • Relation:
      http://annchildneurol.org/upload/pdf/acn-2023-00192.pdf; https://doaj.org/toc/2635-909X; https://doaj.org/toc/2635-9103
    • الرقم المعرف:
      10.26815/acn.2023.00192
    • الرقم المعرف:
      edsdoj.7627c5d210374c95a9a826aab5f7805b