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Q36358411-E8ABF540-1195-4AD9-ADDF-C2CF4694BF40
Q36358411-E8ABF540-1195-4AD9-ADDF-C2CF4694BF40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36358411-E8ABF540-1195-4AD9-ADDF-C2CF4694BF40
A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment
P2860
Q36358411-E8ABF540-1195-4AD9-ADDF-C2CF4694BF40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36358411-E8ABF540-1195-4AD9-ADDF-C2CF4694BF40
rank
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type
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Statement
wasDerivedFrom
987ccb9c2b6d1eb57d9796968f209e82a4563262
P2860
A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.