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Investigation of mitochondrial disease.
Poulton J, Brown GK. Poulton J, et al. Among authors: brown gk. 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.
A national perspective on prenatal testing for mitochondrial disease.
Nesbitt V, Alston CL, Blakely EL, Fratter C, Feeney CL, Poulton J, Brown GK, Turnbull DM, Taylor RW, McFarland R. Nesbitt V, et al. Among authors: brown gk. Eur J Hum Genet. 2014 Nov;22(11):1255-9. doi: 10.1038/ejhg.2014.35. Epub 2014 Mar 19. Eur J Hum Genet. 2014. PMID: 24642831 Free PMC article.
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.
Oláhová M, Hardy SA, Hall J, Yarham JW, Haack TB, Wilson WC, Alston CL, He L, Aznauryan E, Brown RM, Brown GK, Morris AA, Mundy H, Broomfield A, Barbosa IA, Simpson MA, Deshpande C, Moeslinger D, Koch J, Stettner GM, Bonnen PE, Prokisch H, Lightowlers RN, McFarland R, Chrzanowska-Lightowlers ZM, Taylor RW. Oláhová M, et al. Among authors: brown rm, brown gk. Brain. 2015 Dec;138(Pt 12):3503-19. doi: 10.1093/brain/awv291. Epub 2015 Oct 27. Brain. 2015. PMID: 26510951 Free PMC article.
Metabolic disorders of embryogenesis.
Brown GK. Brown GK. J Inherit Metab Dis. 1994;17(4):448-58. doi: 10.1007/BF00711360. J Inherit Metab Dis. 1994. PMID: 7967495 Review.
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