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Q24677029-07FEA1FC-CFFC-4D26-BA72-F55AD6280A01
Q24677029-07FEA1FC-CFFC-4D26-BA72-F55AD6280A01
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http://www.wikidata.org/entity/statement/Q24677029-07FEA1FC-CFFC-4D26-BA72-F55AD6280A01
Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy
P2860
Q24677029-07FEA1FC-CFFC-4D26-BA72-F55AD6280A01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24677029-07FEA1FC-CFFC-4D26-BA72-F55AD6280A01
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wasDerivedFrom
b3e04377e10a1c76ef37391bb5fc58159c3e0fc7
P2860
A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.