Congenital Disorders of Glycosylation

Difficulty: Hard-- Congenital Disorders of Glycosylation is the family of diseases encompassing NGLY1 deficiency. These docs will provide an overview of the general space of related genetic disorders, and treatments identified to these closely related disorders may be relevant to NGLY1 patients. There are over 400 docs in this set, please help mark them up.

Community progress on this set:

Top doc set contributors:
  • billmcquillan

  • ckrypton

  • Isabelle

  • mariomar_it

  • skye

Group Statistics
  1. Total number of contributors: 92

  2. Total documents: 483

  3. Current average f-score: 0.000

  4. Start date: 2015.05.12

  5. End date: 2015.07.29

Top contributor word cloud: