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Human lysozyme gene mutations cause hereditary systemic amyloidosis.
Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ, et al. Pepys MB, et al. Among authors: soutar ak. Nature. 1993 Apr 8;362(6420):553-7. doi: 10.1038/362553a0. Nature. 1993. PMID: 8464497
Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy.
Pepys MB, Tennent GA, Booth DR, Bellotti V, Lovat LB, Tan SY, Persey MR, Hutchinson WL, Booth SE, Madhoo S, Soutar AK, Hawkins PN, Van Zyl-Smit R, Campistol JM, Fraser PE, Radford SE, Robinson CV, Sunde M, Serpell LC, Blake CC. Pepys MB, et al. Among authors: soutar ak. Ciba Found Symp. 1996;199:73-81; discussion 81-9. doi: 10.1002/9780470514924.ch6. Ciba Found Symp. 1996. PMID: 8915605
Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.
Soutar AK, Hawkins PN, Vigushin DM, Tennent GA, Booth SE, Hutton T, Nguyen O, Totty NF, Feest TG, Hsuan JJ, et al. Soutar AK, et al. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7389-93. doi: 10.1073/pnas.89.16.7389. Proc Natl Acad Sci U S A. 1992. PMID: 1502149 Free PMC article.
133 results