In the article that appeared on page 151 of the August 2010 issue of Pediatric Research, panel B of Figure 3 is missing the electropherogram. The correct figure and legend appear below.
Electropherograms showing the TK2 heterozygous mutations found in the patient (arrows). A, Novel mutation (c.276dupA) in exon 2. B, Previously reported mutation (c.730_732delAAG) in exon 8. C and D, Wild-type sequences obtained from a healthy control.
References
Martà R, Nascimento A, Colomer J, Lara MC, López-Gallardo E, Ruiz-Pesini E, Montoya J, Andreu AL, Briones P, Pineda M 2010 Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 Gene. Pediatr Res 68( 2): 151–154
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The online version of the original article can be found at 10.1203/PDR.0b013e3181e33bbe
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Erratum: Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 Gene: Erratum. Pediatr Res 68, 451 (2010). https://doi.org/10.1203/PDR.0b013e3181fd26e8
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DOI: https://doi.org/10.1203/PDR.0b013e3181fd26e8
