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Q44909039-FB86F827-0A23-4EAA-940A-560EF19432BF
Q44909039-FB86F827-0A23-4EAA-940A-560EF19432BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44909039-FB86F827-0A23-4EAA-940A-560EF19432BF
Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A.
P2860
Q44909039-FB86F827-0A23-4EAA-940A-560EF19432BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44909039-FB86F827-0A23-4EAA-940A-560EF19432BF
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wasDerivedFrom
4b033354d5a080a59b417e0452db79672a2b57ef
P2860
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease