Links
[1] http://ghr.nlm.nih.gov/gene/C10orf2
[2] https://disorders.eyes.arizona.edu/disorders/external-ophthalmoplegia-polg-and-mtdna-mutations
[3] http://www.ncbi.nlm.nih.gov/omim/157640
[4] http://www.ncbi.nlm.nih.gov/omim/258450
[5] https://disorders.eyes.arizona.edu/disorders/external-ophthalmoplegia-ant1-and-mtdna-mutations
[6] http://www.ncbi.nlm.nih.gov/omim/609283
[7] https://disorders.eyes.arizona.edu/disorders/spinocerebellar-ataxia-infantile-onset
[8] http://omim.org/entry/271245
[9] https://disorders.eyes.arizona.edu/references/mutations-twinkle-primase-helicase-cause-perrault-syndrome-neurologic-features
[10] https://disorders.eyes.arizona.edu/references/clinical-histochemical-and-molecular-spectrum-peo1twinkle-linked-adpeo
[11] https://disorders.eyes.arizona.edu/references/ant1-twinkle-polg-and-tp-new-genes-open-our-eyes-ophthalmoplegia