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LETTER TO THE EDITOR

Critical reassessment of a five-generation Chinese family carrying deafness-associated mitochondrial 1555A>G mutation

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Pages 1239-1240 | Received 03 Jun 2011, Accepted 16 Jun 2011, Published online: 15 Aug 2011

References

  • Men M, Jiang L, Wang H, Liu Y, Hu Z, He C, Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A>G mutation. Acta Otolaryngol 2011;Apr 19 [Epub ahead of print].
  • Yao YG, Kong QP, Salas A, Bandelt HJ. Pseudomitochondrial genome haunts disease studies. J Med Genet 2008;12:769–72.
  • Salas A, Yao YG, Macaulay V, Vega A, Carracedo A, Bandelt HJ. A critical reassessment of the role of mitochondria in tumorigenesis. PLoS Med 2005;11:e296.
  • Woischnik M, Moraes CT. Pattern of organization of human mitochondrial pseudogenes in the nuclear genome. Genome Res 2002;6:885–93.

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