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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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| Izdano u: | Acta Neuropathol Commun |
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| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2014
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| Teme: | |
| Online pristup: | 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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