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Q41490578-0EED8B1E-A8F0-45FF-B0E6-1BC939F862DD
Q41490578-0EED8B1E-A8F0-45FF-B0E6-1BC939F862DD
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Statement
http://www.wikidata.org/entity/statement/Q41490578-0EED8B1E-A8F0-45FF-B0E6-1BC939F862DD
Novel TGM5 mutations in acral peeling skin syndrome.
P2860
Q41490578-0EED8B1E-A8F0-45FF-B0E6-1BC939F862DD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41490578-0EED8B1E-A8F0-45FF-B0E6-1BC939F862DD
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wasDerivedFrom
2db3c91a773ded479e5e4679b7000a23b4e8809a
P2860
Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A.