Fig. 2From: A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case reportSanger sequencing confirmation of the variants in USH2A identified in this study. a Sequences of the heterozygous splicing variant c.8559-2A>G and the corresponding wild-type sequence. b Sequences of the heterozygous frameshift variant c.4749delT (p.(Phe1583Leufs*10)) and the corresponding wild-type sequenceBack to article page