Glial cells in familial amyloidotic polyneuropathy

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,...

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Udgivet i:Acta Neuropathol Commun
Main Authors: Gonçalves, Nádia Pereira, Costelha, Susete, Saraiva, Maria João
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2014
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4280682/
https://ncbi.nlm.nih.gov/pubmed/25519307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-014-0177-8
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