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Q50525033-DBBC0F33-D09E-487F-ABBD-2DB8B2442688
Q50525033-DBBC0F33-D09E-487F-ABBD-2DB8B2442688
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50525033-DBBC0F33-D09E-487F-ABBD-2DB8B2442688
A novel mutation and unusual clinical features in a patient with immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
P2860
Q50525033-DBBC0F33-D09E-487F-ABBD-2DB8B2442688
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50525033-DBBC0F33-D09E-487F-ABBD-2DB8B2442688
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
c0dc71f0b38607fc19b59eca485a5ca3b9d4c061
P2860
Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes