. . . . . . . . . . . . "[2 mutant alleles of RDX in 2 consanguineous families associated with neurosensory hearing loss; sequence analysis of RDX from original DFNB24 family revealed a c.463C > T transition substitution predicted to truncate radixin in the FERM domain ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:02+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .