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Figure 3 | BMC Medical Genetics

Figure 3

From: MRPS18CP2 alleles and DEFA3absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene

Figure 3

MRPS18CP2 sequence and expression analysis. (A) Alignment of MRPS18CP2 pseudogene with MRPS18C mRNA (GenBank accession number NM_016067). Asterisks indicate sequence changes between the gene mRNA and the chromosome 8p23.1 pseudogene. (B) RT-PCR experiments showing expression of a transcript containing MRPS18CP2 pseudogene in different tissues.

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