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Hereditary fructose intolerance.
Ali M, Rellos P, Cox TM. Ali M, et al. Among authors: cox tm. J Med Genet. 1998 May;35(5):353-65. doi: 10.1136/jmg.35.5.353. J Med Genet. 1998. PMID: 9610797 Free PMC article. Review.
Juvenile hemochromatosis locus maps to chromosome 1q.
Roetto A, Totaro A, Cazzola M, Cicilano M, Bosio S, D'Ascola G, Carella M, Zelante L, Kelly AL, Cox TM, Gasparini P, Camaschella C. Roetto A, et al. Among authors: cox tm. Am J Hum Genet. 1999 May;64(5):1388-93. doi: 10.1086/302379. Am J Hum Genet. 1999. PMID: 10205270 Free PMC article.
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.
Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, Le Gall JY, Halsall DJ, Elsey TS, Kelly A, Cox TM, Clare M, Bomford A, Vandwalle JL, Rochette J, Borot N, Coppin H, Roth MP, Ryan E, Crowe J, Totaro A, Gasparini P, Roetto A, Walker AP, et al. Merryweather-Clarke AT, et al. Among authors: cox tm. Nat Genet. 1999 Nov;23(3):271. doi: 10.1038/15452. Nat Genet. 1999. PMID: 10545942 No abstract available.
Human glucocerebrosidase mediates formation of xylosyl-cholesterol by β-xylosidase and transxylosidase reactions.
Boer DE, Mirzaian M, Ferraz MJ, Zwiers KC, Baks MV, Hazeu MD, Ottenhoff R, Marques ARA, Meijer R, Roos JCP, Cox TM, Boot RG, Pannu N, Overkleeft HS, Artola M, Aerts JM. Boer DE, et al. Among authors: cox tm. J Lipid Res. 2021 Jan 6;62:100018. doi: 10.1194/jlr.RA120001043. Online ahead of print. J Lipid Res. 2021. PMID: 33361282 Free article.
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