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Fig. 4 | BMC Medical Genomics

Fig. 4

From: A novel homozygous TUB mutation associated with autosomal recessive retinitis pigmentosa in a consanguineous Chinese family

Fig. 4

Minigene assay for the c.1379 A > G variant in TUB. A Schematic illustration of cloned vectors (pMini-CopGFP-TUB minigene), red * indicates the variant site. B Electrophoresis of RT-PCR fragments from APRE-19 cells and 293 T cells (original gel is presented in Additional file 1: Fig. S2). C Splicing sequences confirmed by Sanger sequencing. D Schematic diagram shows no effect of the Tub variant (c.1379A > G) on splicing. WT, wild-type; MT, mutant-type

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