Clinical Study

Whole Exome Sequencing Reveals Genetic Predisposition in a Large Family with Retinitis Pigmentosa

Figure 3

Chromatography of the identified mutation in each patient. Sanger sequencing results obtained from seven affected members (III-2, III-7, III-10, III-13, III-16, IV-2, and IV-10) and an unaffected member (III-4) in the Chinese family.
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