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Fig. 4 | BMC Medical Genetics

Fig. 4

From: Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family

Fig. 4

Results form CHST6 Sanger Sequencing. Electropherograms from Sanger sequencing indicating homozygous E71Q genotype in the two affected sisters (IV.3 and IV.4), heterozygous genotype in the carrier mother (III.8) and homozygous reference genotype in the unaffected brother (IV.1). The red arrow indicates the position of the E71Q mutation and the sequences are given for the reverse strand

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