Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish population.

Human heredity - 1 Jan 1992

Drugge U, Holmgren G, Udd B

Abstract excerpt

Finnish hereditary amyloidosis-Meretoja (FAP type 4) is the predominating type of hereditary amyloidosis in the Finnish population, found in more than 200 individuals. We present a Finnish family with familial amyloidotic polyneuropathy (FAP Met30), a type of amyloidosis hitherto not described in the Finnish population. Genealogical tracing back to the 18th century revealed no connections with Swedish FAP...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Amyloidosis
Share to Finland

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

Share to FAP gene

Share to Mutation

Share to Pedigree

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 1511998
DOI: 10.1159/000154064

Genes

FAP

Provenance

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish population.PMID 1511998Read ↗

Hereditary amyloidosis of the Finnish type in a German family: clinical and electrophysiological presentation.Semantic proximity Read ↗

Regional difference and similarity of familial amyloidosis with polyneuropathy in France.Semantic proximity Read ↗

Familial amyloidosis of the Finnish type (FAF). A clinical study of 30 patients.Semantic proximity Read ↗

Familial amyloidosis of the Finnish type: clinical and neurophysiological features of two index cases.Semantic proximity Read ↗

Late-onset familial amyloid polyneuropathy (FAP) Val30Met without family history.Semantic proximity Read ↗

[Familial amyloidotic polyneuropathies].Semantic proximity Read ↗

Familial amyloidosis with polyneuropathy type 1 caused by transthyretin mutation Val50Met (Val30Met): 4 cases in a non-endemic area.Semantic proximity Read ↗

Transthyretin-related Familial Amyloid Polyneuropathy (TTR-FAP) caused by a very rare, de novo mutation in a Polish patient.Semantic proximity Read ↗

TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patients.Semantic proximity Read ↗

Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families.Semantic proximity Read ↗

Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant.Semantic proximity Read ↗

Japanese monozygotic twins with familial amyloidotic polyneuropathy (FAP) (ATTR Val30Met).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.