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Article

Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy.

Journal of medical genetics - 1 Apr 2004

Ohmori H, Ando Y, Makita Y, Onouchi Y, Nakajima T, Saraiva M J M, Terazaki H, Suhr O, Sobue G, Nakamura M, Yamaizumi M, Munar-Ques M, Inoue I, Uchino M, Hata A

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Share to Amino Acid Substitution
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Share to Amyloid Neuropathies, Familial

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Identifiers

PMID: 15060127
DOI: 10.1136/jmg.2003.014803
PMCID: PMC1735751

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.

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Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy.PMID 15060127Read ↗

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Amyloidogenic transthyretin Val30Met homozygote showing unusually early-onset familial amyloid polyneuropathy.Semantic proximity Read ↗

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