Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 660 citations

Life Sciences, Genetics, Molecular Biology +12

A stop-codon mutation in the BRI gene associated with familial British dementia

Rubén Vidal, Blas Frangione, Agueda Rostagno et al. · Nature · 1999 · 473 citations

Life Sciences, Genetics, Molecular Genetics +16

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy.

Paulo Costa, A S Figueira, Fernanda Bravo · Proceedings of the National Academy of Sciences · 1978 · 427 citations · Full text

Life Sciences, Biochemistry, Neurology +17

Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C).

Jorge Ghiso, O Jensson, Blas Frangione · Proceedings of the National Academy of Sciences · 1986 · 335 citations · Full text

Life Sciences, Biochemistry, Pathology +17

A decamer duplication in the 3′ region of the <i>BRI</i> gene originates an amyloid peptide that is associated with dementia in a Danish kindred

Rubén Vidal, Tamás Révész, Agueda Rostagno et al. · Proceedings of the National Academy of Sciences · 2000 · 305 citations

Life Sciences, Genetics, Neurology +17