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Figure 2 | BMC Medical Genetics

Figure 2

From: Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome

Figure 2

Mutation analysis of GJB2 in the two Cameroonian individuals affected with sporadic KID. Panel A: Sequence chromatograms of GJB2 from unaffected individual; Panel B: Sequence chromatograms from affected patients depicting the heterozygous transition 148G → A at codon 50 encoding asparagine instead of aspartic acid (p.Asp50Asn) (Panel B).

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BMC Medical Genetics

ISSN: 1471-2350

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