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Mitochondrial DNA and genetic disease.
Poulton J. Poulton J. Dev Med Child Neurol. 1993 Sep;35(9):833-40. doi: 10.1111/j.1469-8749.1993.tb11736.x. Dev Med Child Neurol. 1993. PMID: 7689068 Review. No abstract available.
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
Livesey KJ, Wimhurst VL, Carter K, Worwood M, Cadet E, Rochette J, Roberts AG, Pointon JJ, Merryweather-Clarke AT, Bassett ML, Jouanolle AM, Mosser A, David V, Poulton J, Robson KJ. Livesey KJ, et al. Among authors: poulton j. J Med Genet. 2004 Jan;41(1):6-10. doi: 10.1136/jmg.2003.008805. J Med Genet. 2004. PMID: 14729817 Free PMC article.
Mitochondrial DNA: does more lead to less?
Poulton J, Holt IJ. Poulton J, et al. Nat Genet. 1994 Dec;8(4):313-5. doi: 10.1038/ng1294-313. Nat Genet. 1994. PMID: 7894476 No abstract available.
Investigation of mitochondrial disease.
Poulton J, Brown GK. Poulton J, et al. Arch Dis Child. 1995 Aug;73(2):94-7. doi: 10.1136/adc.73.2.94-a. Arch Dis Child. 1995. PMID: 7574881 Free PMC article. Review. No abstract available.
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