APCDG - Congenital Disorders of Glycosylation
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Summary on PMM2-CDG available

25/10/2015

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Report done by Pf Freeze PhD, Professor and Director, Genetic Disease Program, Sanford Children's Health Research Center, Sanford-Burnham Medical Research Institute available at NORD website: https://rarediseases.org/rare-diseases/pmm2-cdg/

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Appsolutely Engaging and Educational: iPad Apps for Children with Visual Impairments and Special Needs

25/10/2015

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©2015 Portuguese Association for CDG and other Rare Metabolic Diseases (APCDG-DMR)
Contact us: sindromecdg@gmail.com
  • About US
    • What we do
    • Who we help
  • Research
  • Resources
    • Rare CDG
    • Publications
    • Guia Metabolica
    • CDG Facts
    • Task Force CDG Communication >
      • ALG1-CDG (CDG Ik)
      • PMM2-CDG (CDG Ia)
      • PGM1-CDG (CDG It)
      • ALG6-CDG (CDG Ic)
  • EDUCATION
  • Awareness
    • Get involved World CDG Awareness Day 2018 >
      • Go Social World CDG Awareness Day
      • Spread World CDG Awareness Day
      • Plan An Event World CDG Awareness Day
      • Frame your CDG Awareness Campaign
      • Go green! Think CDG! ©Campaign
      • Volunteer World CDG Awareness Day
      • Press kit World CDG Awareness Day
    • Map of events for World CDG Awareness Day 2018
    • CrowdCDG
    • Awareness Day 2017
    • Awareness Day 2016
    • Rare Diseases
  • Community
    • Join Us - Membership
    • CDG Patient Groups
    • Empowerment
  • Events
    • Speakers - World Conference on CDG
    • Registrations - World Conference on CDG
    • Follow up - World Conference on CDG
  • DONATE
  • BLOG
  • New Page