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Q48005661-10FECE82-045D-4CE2-9E49-532C06D05889
Q48005661-10FECE82-045D-4CE2-9E49-532C06D05889
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Statement
http://www.wikidata.org/entity/statement/Q48005661-10FECE82-045D-4CE2-9E49-532C06D05889
Novel mutation (p.L91P, c.272T>C) of keratin 17 in a case with pachyonychia congenita type 2.
P2860
Q48005661-10FECE82-045D-4CE2-9E49-532C06D05889
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48005661-10FECE82-045D-4CE2-9E49-532C06D05889
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wasDerivedFrom
4267894178e2b7c60868e2723828447949da019c
P2860
A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2