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Q34560844-8D91F545-ACBC-4FCF-AF2E-76CA4D41CDC0
Q34560844-8D91F545-ACBC-4FCF-AF2E-76CA4D41CDC0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34560844-8D91F545-ACBC-4FCF-AF2E-76CA4D41CDC0
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42
P2860
Q34560844-8D91F545-ACBC-4FCF-AF2E-76CA4D41CDC0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34560844-8D91F545-ACBC-4FCF-AF2E-76CA4D41CDC0
rank
NormalRank
type
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wasDerivedFrom
0c0a5f01da8c5dc52b350a62b806a6d75048ef99
P2860
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.