Two variants in MYO7A (NM_000260.3) were identified: c.1344-2A > G (splicing site mutation reported in ClinVar for Usher Syndrome type I, either in homozygous or compound heterozygous state; rs111033415), in trans with the novel nonsense variant c.733C > T, p.(Gln245*). Here, MYO7A is linked to Usher syndrome type 1.