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• ALG1-CDG
  == ALG1-CDG == ...G), also known as '''Congenital disorder of glycosylation type Ik''' or '''CDG-Ik''', is a rare genetic disorder that affects the body's ability to proper
  2 KB (270 words) - 23:15, 3 February 2024
• MPI-CDG
  '''MPI-CDG''' '''MPI-CDG''' (''pronunciation: em-pi-si-di-ji''), also known as '''Mannose-Phosphate
  2 KB (198 words) - 01:21, 5 February 2024
• SRD5A3-CDG
  == SRD5A3-CDG == '''SRD5A3-CDG''' (pronounced as S-R-D-Five-A-Three-C-D-G) is a rare congenital disorder o
  2 KB (236 words) - 04:46, 6 February 2024

Page text matches

• ALG1-CDG
  == ALG1-CDG == ...G), also known as '''Congenital disorder of glycosylation type Ik''' or '''CDG-Ik''', is a rare genetic disorder that affects the body's ability to proper
  2 KB (270 words) - 23:15, 3 February 2024
• SRD5A3-CDG
  == SRD5A3-CDG == '''SRD5A3-CDG''' (pronounced as S-R-D-Five-A-Three-C-D-G) is a rare congenital disorder o
  2 KB (236 words) - 04:46, 6 February 2024
• Congenital disorders of glycosylation
  ...ssembly of the sugar chain (the [[oligosaccharide]]), while Type II CDG ([[CDG-II]]) involves defects in the processing of the sugar chain. Each type is f
  2 KB (279 words) - 22:19, 13 February 2024
• MPI-CDG
  '''MPI-CDG''' '''MPI-CDG''' (''pronunciation: em-pi-si-di-ji''), also known as '''Mannose-Phosphate
  2 KB (198 words) - 01:21, 5 February 2024