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Q36685396-BC04C75F-1832-4533-B061-1AFFA6DBAF7C
Q36685396-BC04C75F-1832-4533-B061-1AFFA6DBAF7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36685396-BC04C75F-1832-4533-B061-1AFFA6DBAF7C
Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.
P2860
Q36685396-BC04C75F-1832-4533-B061-1AFFA6DBAF7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36685396-BC04C75F-1832-4533-B061-1AFFA6DBAF7C
rank
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type
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Statement
wasDerivedFrom
4f52ecb4d40ad5532ef3af71aea7d4b2bde1426d
P2860
Human keratin diseases: hereditary fragility of specific epithelial tissues.