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Fig. 3 | BMC Ophthalmology

Fig. 3

From: Mutation screening of the USH2A gene reveals two novel pathogenic variants in Chinese patients causing simplex usher syndrome 2

Fig. 3

Pedigree of the Chinese Usher syndrome type II patients’ family. The black filled shapes mean individuals diagnosed with USH2 and the unfilled mean unaffected ones. Males are represented by squares, females circles. Patient number is below the individuals’ symbol. Individuals with available DNA samples were marked with asterisk. Question mark means the unknown allelic variant. M1: c.4217C > A (p.Ser1406X); M2: c.8232G > C (p.Trp2744Cys); M3: c.8559-2A > G; M4: c.11389 + 3A > T; M5: c.11780A > G (p.Asp3927Gly)

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