Učitavanje...

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,...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Acta Neuropathol Commun
Glavni autori: Gonçalves, Nádia Pereira, Costelha, Susete, Saraiva, Maria João
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2014
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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!