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A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.
Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM. Taylor RW, et al. Among authors: turnbull dm. J Am Coll Cardiol. 2003 May 21;41(10):1786-96. doi: 10.1016/s0735-1097(03)00300-0. J Am Coll Cardiol. 2003. PMID: 12767666 Free article.
The neurology of mitochondrial DNA disease.
McFarland R, Taylor RW, Turnbull DM. McFarland R, et al. Among authors: turnbull dm. Lancet Neurol. 2002 Oct;1(6):343-51. doi: 10.1016/s1474-4422(02)00159-x. Lancet Neurol. 2002. PMID: 12849395 Review.
The diagnosis of mitochondrial muscle disease.
Taylor RW, Schaefer AM, Barron MJ, McFarland R, Turnbull DM. Taylor RW, et al. Among authors: turnbull dm. Neuromuscul Disord. 2004 Apr;14(4):237-45. doi: 10.1016/j.nmd.2003.12.004. Neuromuscul Disord. 2004. PMID: 15019701 Review.
Neuropathological aspects of mitochondrial DNA disease.
Betts J, Lightowlers RN, Turnbull DM. Betts J, et al. Among authors: turnbull dm. Neurochem Res. 2004 Mar;29(3):505-11. doi: 10.1023/b:nere.0000014821.07269.8d. Neurochem Res. 2004. PMID: 15038598 Review.
Strategies for treating disorders of the mitochondrial genome.
Smith PM, Ross GF, Taylor RW, Turnbull DM, Lightowlers RN. Smith PM, et al. Among authors: turnbull dm. Biochim Biophys Acta. 2004 Dec 6;1659(2-3):232-9. doi: 10.1016/j.bbabio.2004.09.003. Biochim Biophys Acta. 2004. PMID: 15576056 Free article. Review.
600 results