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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Acta Neuropathol Commun
Main Authors: Gonçalves, Nádia Pereira, Costelha, Susete, Saraiva, Maria João
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2014
Teme:
Research
Online dostop: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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