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Article

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.

Genomics - 1 Jul 1992

Maury C P, Kere J, Tolvanen R, de la Chapelle A

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 1322360
DOI: 10.1016/0888-7543(92)90183-s

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.PMID 1322360Read ↗

Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis.Semantic proximity Read ↗

Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implications.Semantic proximity Read ↗

[Finnish hereditary amyloidosis: a mutation in the gelsolin gene].Semantic proximity Read ↗

Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide.Semantic proximity Read ↗

Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)Semantic proximity Read ↗

Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187.Semantic proximity Read ↗

Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.Semantic proximity Read ↗

Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East.Semantic proximity Read ↗

Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.Semantic proximity Read ↗

A molecular perspective of gelsolin amyloidosis: An old foe with new faces.Semantic proximity Read ↗

Mutation in gelsolin gene in Finnish hereditary amyloidosis.Semantic proximity Read ↗

Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.Semantic proximity Read ↗

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