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Disease Markers
Volume 30, Issue 6, Pages 283-289
http://dx.doi.org/10.3233/DMA-2011-0786

Detection of Deafness-Causing Mutations in the Greek Mitochondrial Genome

Haris Kokotas,1 Maria Grigoriadou,1 George S. Korres,1 Elisabeth Ferekidou,1 Dimitrios Kandiloros,2 Stavros Korres,3 and Michael B. Petersen1

1Department of Genetics, Institute of Child Health, ‘Aghia Sophia’ Children’s Hospital, Athens, Greece
2Department of Otorhinolaryngology – Head and Neck Surgery, Athens University Medical School, Attiko Hospital, Athens, Greece
3Department of Otorhinolaryngology – Head and Neck Surgery, Athens University Medical School, Hippokration Hospital, Athens, Greece

Received 28 June 2011; Accepted 28 June 2011

Copyright © 2011 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Haris Kokotas, Maria Grigoriadou, George S. Korres, et al., “Detection of Deafness-Causing Mutations in the Greek Mitochondrial Genome,” Disease Markers, vol. 30, no. 6, pp. 283-289, 2011. https://doi.org/10.3233/DMA-2011-0786.