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1
s12967-016-0780-5
s12967-016-0780-5
https://scigraph.springernature.com/pub.10.1186/s12967-016-0780-5
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss
P2888
Q27303610-25BD936A-9A93-4DF5-8DC8-4ED5CF973BD1
P2888
s12967-016-0780-5
https://scigraph.springernature.com/pub.10.1186/s12967-016-0780-5