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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Detalles Bibliográficos
Autores principales: Gonçalves, Nádia Pereira, Costelha, Susete, Saraiva, Maria João
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280682/
https://www.ncbi.nlm.nih.gov/pubmed/25519307
http://dx.doi.org/10.1186/s40478-014-0177-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280682/
https://www.ncbi.nlm.nih.gov/pubmed/25519307
http://dx.doi.org/10.1186/s40478-014-0177-8

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