Genetics Research International / 2011 / Article / Fig 1

Research Article

Molecular Investigation of Pediatric Portuguese Patients with Sensorineural Hearing Loss

Figure 1

Schematic secondary structure of the wild-type human mitochondrial tRNATrp gene showing the reported variants found in this gene. Black stands for pathogenic mutations, gray stands for polymorphic mutations, and red stands for the novel mutation described in our study.
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