Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease
- 1 July 1992
- Vol. 13 (3) , 902-903
- https://doi.org/10.1016/0888-7543(92)90183-s
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Familial amyloidosis, Finnish type: G654 → A mutation of the gelsolin gene in Finnish families and an unrelated American familyGenomics, 1992
- Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.Journal of Clinical Investigation, 1991
- Gelsolin variant (Asn-187) in familial amyloidosis, Finnish typeBiochemical Journal, 1990
- Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin geneFEBS Letters, 1990
- Mutation in gelsolin gene in Finnish hereditary amyloidosis.The Journal of Experimental Medicine, 1990
- Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolinBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1990
- Finnish hereditary amyloidosisFEBS Letters, 1990