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Article

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

Genomics - 1 May 1992

Paunio T, Kiuru S, Hongell V, Mustonen E, Syvänen A C, Bengström M, Palo J, Peltonen L

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

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PMID: 1315718
DOI: 10.1016/0888-7543(92)90235-k

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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.

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis.PMID 1315718Read ↗

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

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

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

Atypical Presentation of Gelsolin Amyloidosis in a Man of African Descent with a Novel Mutation in the Gelsolin Gene.Semantic proximity Read ↗

A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish type.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 amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.Semantic proximity Read ↗

Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation.Semantic proximity Read ↗

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

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