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Q46445421-9A22FB2E-44F6-4578-8ED9-CA0E01C31DCC
Q46445421-9A22FB2E-44F6-4578-8ED9-CA0E01C31DCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46445421-9A22FB2E-44F6-4578-8ED9-CA0E01C31DCC
A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.
P2860
Q46445421-9A22FB2E-44F6-4578-8ED9-CA0E01C31DCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46445421-9A22FB2E-44F6-4578-8ED9-CA0E01C31DCC
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d1bad2086241f588a91cc076eae4f5eb58d1b69e
P2860
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.