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1
S00508-017-1230-Y
S00508-017-1230-Y
http://dx.doi.org/10.1007/S00508-017-1230-Y
Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss.
P356
Q38653445-B4E6CE57-D178-4ECF-9495-402DE5CBAA81
P356
S00508-017-1230-Y
http://dx.doi.org/10.1007/S00508-017-1230-Y