Inherited amyloidosis.

This publication has 12 references indexed in Scilit:

• A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy
  Genomics, 1990
• A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases
  Biochemical and Biophysical Research Communications, 1990
• Finnish hereditary amyloidosis
  FEBS Letters, 1990
• Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences
  Clinical Genetics, 1990
• A new mutation causing familial amyloidotic polyneuropathy
  Biochemical and Biophysical Research Communications, 1989
• Variant apolipoprotein AI as a major constituent of a human hereditary amyloid
  Biochemical and Biophysical Research Communications, 1988
• Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain
  Nature, 1986
• Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome.
  1969
• Familial primary amyloidosis with severe amyloid heart disease
  The American Journal of Medicine, 1962
• A PECULIAR FORM OF PERIPHERAL NEUROPATHY
  Brain, 1952