Hereditary renal amyloidosis associated with a mutant fibrinogen α–chain
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0393-252.pdf
Reference22 articles.
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3. Nichols, W.C., Gregg, R.E., Brewer, Jr., B. & Benson, M.D. A mutation in apolipoprotein A-1 in the Iowa Type of familial amyloidotic polyneuropathy. Genomics 8, 318–323 (1990).
4. Maury, C.P.J., Kere, J., Tolvanen, R. & de la Chapelle, A. Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene. FEBS Lett. 276, 75–77 (1990).
5. Levy, E. et al. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J. exp. Med. 172, 1865–1867 (1990).
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