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Article

A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.

Human mutation - 1 Jan 1994

Ferlini A, Patrosso M C, Repetto M, Frattini A, Villa A, Fini S, Salvi F, Vezzoni P, Forabosco A

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Source

Identifiers

PMID: 7951260
DOI: 10.1002/humu.1380040110

Genes

TTR

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.

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A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.PMID 7951260Read ↗

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Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.Semantic proximity Read ↗

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A new transthyretin mutation associated with amyloid cardiomyopathy.Semantic proximity Read ↗

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