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Article

Glial cells in familial amyloidotic polyneuropathy.

Acta neuropathologica communications - 18 Dec 2014

Gonçalves Nádia P, Costelha Susete, Saraiva Maria J

Abstract excerpt

INTRODUCTION: Transthyretin V30M mutation is the most common variant leading to Familial Amyloidotic Polyneuropathy. In this genetic disorder, Transthyretin accumulates preferentially in the extracellular matrix of peripheral and autonomic nervous systems leading to cell death and dysfunction. Thus, knowledge regarding important biological systems for Transthyretin clearance might unravel novel insights into...

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Identifiers

PMID: 25519307
DOI: 10.1186/s40478-014-0177-8
PMCID: PMC4280682

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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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