KEGG   VARIANT: 729920v1
Entry
729920v1                      Variant                              
Name
ISPD deficiency
Gene
CRPPA  CDP-L-ribitol pyrophosphorylase A [KO:K21031]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 614631
Network
nt06013  O-Glycan biosynthesis
Disease
H01959  Muscular dystrophy-dystroglycanopathy type C
Reference
  Authors
Roscioli T, Kamsteeg EJ, Buysse K, Maystadt I, van Reeuwijk J, van den Elzen C, van Beusekom E, Riemersma M, Pfundt R, Vissers LE, Schraders M, Altunoglu U, Buckley MF, Brunner HG, Grisart B, Zhou H, Veltman JA, Gilissen C, Mancini GM, Delree P, Willemsen MA, Ramadza DP, Chitayat D, Bennett C, Sheridan E, Peeters EA, Tan-Sindhunata GM, de Die-Smulders CE, Devriendt K, Kayserili H, El-Hashash OA, Stemple DL, Lefeber DJ, Lin YY, van Bokhoven H
  Title
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-dystroglycan.
  Journal
Nat Genet 44:581-5 (2012)
DOI:10.1038/ng.2253
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