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Q36742584-4C13C24F-E900-48F6-AD0F-B26A687BEBF2
Q36742584-4C13C24F-E900-48F6-AD0F-B26A687BEBF2
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Statement
http://www.wikidata.org/entity/statement/Q36742584-4C13C24F-E900-48F6-AD0F-B26A687BEBF2
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease
P2860
Q36742584-4C13C24F-E900-48F6-AD0F-B26A687BEBF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36742584-4C13C24F-E900-48F6-AD0F-B26A687BEBF2
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wasDerivedFrom
204cbf37457e2182f85255110953b2114ccedbcb
P2860
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p