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00016489.2010.506885
00016489.2010.506885
http://dx.doi.org/10.3109/00016489.2010.506885
Impaired membrane targeting and aberrant cellular localization of human Cx26 mutants associated with inherited recessive hearing loss.
P356
Q50436454-215010A2-E7C1-4CEE-897C-C10133F0761F
P356
00016489.2010.506885
http://dx.doi.org/10.3109/00016489.2010.506885