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Genotype-Phenotype Correlations in Alternating Hemiplegia

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اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • بيانات النشر:
      Pediatric Neurology Briefs Publishers
    • الموضوع:
      2014
    • Collection:
      Pediatric Neurology Briefs (E-Journal)
    • نبذة مختصرة :
      Researchers at the National Center of Neurology and Psychiatry, Kodaira, and multiple centers in Japan, analyze the clinical features and ATP1A3 mutations in 35 Japanese children diagnosed with alternating hemiplegia of childhood (AHC).
    • File Description:
      application/xml; application/pdf
    • Relation:
      https://account.pediatricneurologybriefs.com/index.php/up-j-pnb/article/view/pedneurbriefs-28-4-8/348; https://account.pediatricneurologybriefs.com/index.php/up-j-pnb/article/view/pedneurbriefs-28-4-8/349; https://account.pediatricneurologybriefs.com/index.php/up-j-pnb/article/view/pedneurbriefs-28-4-8
    • الرقم المعرف:
      10.15844/pedneurbriefs-28-4-8
    • الدخول الالكتروني :
      https://account.pediatricneurologybriefs.com/index.php/up-j-pnb/article/view/pedneurbriefs-28-4-8
      https://doi.org/10.15844/pedneurbriefs-28-4-8
    • Rights:
      Copyright (c) 2014 The Author(s) ; https://creativecommons.org/licenses/by/4.0
    • الرقم المعرف:
      edsbas.2A7F1A91