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Maternally inherited mitochondrial DNA disease in consanguineous families.
Alston CL, He L, Morris AA, Hughes I, de Goede C, Turnbull DM, McFarland R, Taylor RW. Alston CL, et al. Among authors: taylor rw. Eur J Hum Genet. 2011 Dec;19(12):1226-9. doi: 10.1038/ejhg.2011.124. Epub 2011 Jun 29. Eur J Hum Genet. 2011. PMID: 21712854 Free PMC article.
Insulin sensitivity and mitochondrial gene mutation.
Walker M, Taylor RW, Stewart MW, Bindoff LA, Jackson MJ, Alberti GK, Turnbull DM. Walker M, et al. Among authors: taylor rw. Diabetes Care. 1995 Feb;18(2):273-5. doi: 10.2337/diacare.18.2.273. Diabetes Care. 1995. PMID: 7729311 No abstract available.
Complex aetiology of type 2 diabetes.
Walker M, Taylor R, Armstrong M, Turnbull DM. Walker M, et al. Br J Hosp Med. 1994 Aug 17-Sep 6;52(4):179. Br J Hosp Med. 1994. PMID: 8000686 No abstract available.
Defects of oxidative phosphorylation in man.
Taylor RW, Birch-Machin MA, Lowerson S, Sherratt HS, West IC, Bartlett K, Turnbull DM. Taylor RW, et al. Biochem Soc Trans. 1993 Aug;21 ( Pt 3)(3):804-7. doi: 10.1042/bst0210804. Biochem Soc Trans. 1993. PMID: 8224514 Review. No abstract available.
987 results