Author:
Gillmore J.D.,Booth D.R.,Rela M.,Heaton N.D.,Rahman V.,Stangou A.J.,Pepys M.B.,Hawkins P.N.
Publisher
Oxford University Press (OUP)
Reference35 articles.
1. Pepys MB. Amyloidosis. In: Weatherall DJ, Ledingham JGG, Warrell DA, eds. Oxford Textbook of Medicine, 3rd edn. Oxford, Oxford University Press, 1995:1512–24.
2. Jones LA, Harding JA, Cohen AS, Skinner M. New USA family has apolipoprotein AI (Arg26) variant. In: Natvig JB, Førre Ø, Husby G, Husebekk A, Skogen B, Sletten K, Westermark P, eds. Amyloid and Amyloidosis 1990. Dordrecht, Kluwer Academic Publishers, 1991:385–8.
3. Soutar AK, Hawkins PN, Vigushin DM, Tennent GA, Booth SE, Hutton T, Nguyen O, Totty NF, Feest TG, Hsuan JJ, Pepys MB. Apolipoprotein AI mutation Arg‐60 causes autosomal dominant amyloidosis. Proc Natl Acad Sci USA1992; 89:7389–93.
4. Booth DR, Tan SY, Booth SE, Hsuan JJ, Totty NF, Nguyen O, Tennent GA, Hutchinson WL, Vigushin DM, Thomson N, Soutar AK, Hawkins PN, Pepys MB. Hereditary renal amyloidosis caused by a new apolipoprotein AI variant, Trp50Arg. Nephrol Dial Transplant1995; 10:943.
5. Booth DR, Tan SY, Booth SE, Tennent GA, Hutchinson WL, Hsuan JJ, Totty NF, Nguyen O, Soutar AK, Hawkins PN, Bruguera M, Caballería J, Solé M, Campistol JM, Pepys MB. Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene. J Clin Invest1996; 97:2714–21.
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