Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type

This publication has 33 references indexed in Scilit:

• Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases.
  The Journal of Experimental Medicine, 1989
• Haplotype analysis of familial amyloidotic polyneuropathy
  Human Genetics, 1989
• The gelsolin (GSN) cDNA clone, from 9q32-34, identifies Bell and StuI RFLPs
  Nucleic Acids Research, 1989
• Nucleotide sequence of pig plasma gelsolin: Comparison of protein sequence with human gelsolin and other actin-severing proteins shows strong homologies and evidence for large internal repeats
  Journal of Molecular Biology, 1988
• Gelsolin has three actin-binding sites.
  The Journal of cell biology, 1988
• Structure and biosynthesis of cytoplasmic and secreted variants of gelsolin.
  Journal of Biological Chemistry, 1984
• 3 FORMS OF DOMINANT AMYLOID NEUROPATHY
  1981
• Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.
  Journal of Neurology, Neurosurgery & Psychiatry, 1979
• Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy
  Clinical Genetics, 1973
• Comparative Histopathological and Clinical Findings in Eyes with Lattice Corneal Dystrophy of two Different Types
  Ophthalmologica, 1972