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Amyloid precursor protein haploinsufficiency preferentially mediates brain iron accumulation in mice transgenic for the Huntington’s disease mutation.

BACKGROUND: Huntington’s disease (HD) is an autosomal dominant disorder caused by a CAG expansion in the huntingtin gene that results in expression of mutant huntingtin protein. Iron accumulates in HD brain neurons. Amyloid precursor protein (APP) promotes neuronal iron export. However, the role of...

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Bibliografiske detaljer
Udgivet i:J Huntingtons Dis
Main Authors: Berggren, Kiersten, Agrawal, Sonal, Fox, Julia A., Hildenbrand, Justin, Nelson, Ryan, Bush, Ashley I., Fox, Jonathan H.
Format: Artigo
Sprog:Inglês
Udgivet: 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6594052/
https://ncbi.nlm.nih.gov/pubmed/28550267
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JHD-170242
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