High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients

An intronic expansion of a hexanucleotide GGGGCC repeat in the C9ORF72 gene has recently been shown to be an important cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in familial and sporadic cases. The frequency has only been defined in a small number of populations w...

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Bibliografski detalji
Glavni autori: Mok, Kin Y., Koutsis, Georgios, Schottlaender, Lucia V., Polke, James, Panas, Marios, Houlden, Henry
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2012
Teme:
Genetic Reports Abstract
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3657168/
https://ncbi.nlm.nih.gov/pubmed/22445326
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2012.02.021
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