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Fig. 3 | Journal of Medical Case Reports

Fig. 3

From: Clinical and whole exome sequencing findings in children from Yunnan Yi minority ethnic group with retinitis pigmentosa: two case reports

Fig. 3

Mutations identified by Sanger sequencing analysis in families 1 and 2. A RDH12 c.524C > T variant of the proband in family 1. Arrows denote the mutations. B The unaffected father in family 1. C The unaffected mother in family 1. D PRPF4 c.1273G > A variant of the proband in family 2. Arrows denote the mutations. E The unaffected father in family 2. F The unaffected mother in family 2

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Journal of Medical Case Reports

ISSN: 1752-1947