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Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

Figure 1

Pedigree of Chinese Family 7162 with Recessive USH1 and segregation of the mutations in MYO7A.

The proband is indicated by an arrow. Subject I:1, I:2, II:1, II:2, II:3 and II:4 were tested by NGS. gDNA from II:5 is not available.

Figure 1

doi: https://doi.org/10.1371/journal.pone.0103415.g001