2 results for author:"Vigushin D.M." in Literature citations
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| Human lysozyme gene mutations cause hereditary systemic amyloidosis. Pepy M.B., Hawkins P.N., Booth D.R., Vigushin D.M., Tennent G.A., Soutar A.K., Totty N., Nguyen O., Blake C.C.F., Terry C.J. et al. |
| Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Soutar A.K., Hawkins P.N., Vigushin D.M., Tennent G.A., Booth S.E., Hutton T., Nguyen O., Totty N.F., Feest T.G., Hsuan J.J. et al. Proc. Natl. Acad. Sci. U.S.A. 89:7389-7393(1992) · UniProtKB (1) |