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Details
Link-It Detail - PubMed - Glycogen storage disease type IX: High variability in clinical phenotype.
Debug Stats
  • ### Total Build Time: 6 ms 3.882 KB
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  • Reload Stats
PubMed (1)
Glycogen storage disease type IX: High variability in clinical phenotype. 17689125
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanPHKG25261phosphorylase kinase, gamma 2 (testis)
PUBMED, Pubmed Id: 17689125, PUBMED ID: 17689125
HumanPHKB5257phosphorylase kinase, beta
PUBMED, Pubmed Id: 17689125, PUBMED ID: 17689125
HumanPHKA25256phosphorylase kinase, alpha 2 (liver)
PUBMED, Pubmed Id: 17689125, PUBMED ID: 17689125
XRefs (1)

XRef Types:
pubmed : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
PUBMEDimg 17689125Glycogen storage disease type IX: High variability in clinical phenotype.0self