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Mitochondrial DNA deletion in "identical" twin brothers.
Blakely EL, He L, Taylor RW, Chinnery PF, Lightowlers RN, Schaefer AM, Turnbull DM. Blakely EL, et al. Among authors: schaefer am. J Med Genet. 2004 Feb;41(2):e19. doi: 10.1136/jmg.2003.011296. J Med Genet. 2004. PMID: 14757869 Free PMC article. No abstract available.
The diagnosis of mitochondrial muscle disease.
Taylor RW, Schaefer AM, Barron MJ, McFarland R, Turnbull DM. Taylor RW, et al. Among authors: schaefer am. Neuromuscul Disord. 2004 Apr;14(4):237-45. doi: 10.1016/j.nmd.2003.12.004. Neuromuscul Disord. 2004. PMID: 15019701 Review.
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation.
Deschauer M, Chinnery PF, Schaefer AM, Turnbull DM, Taylor RW, Zierz S, Shanske S, DiMauro S, Majamaa K, Wilichowski E, Thorburn DR. Deschauer M, et al. Among authors: schaefer am. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1204-5. doi: 10.1136/jnnp.2003.026278. J Neurol Neurosurg Psychiatry. 2004. PMID: 15258237 Free PMC article. No abstract available.
151 results