Characterisation of a novel NR4A2 mutation in Parkinson’s disease brain

OBJECTIVE: We performed a mutation screen of NR4A2 (also known as NURR1) in 409 Parkinson’s disease (PD) patients. We identified a novel single base substitution in the 5′UTR of the NR4A2 (also known as NURR1) gene (c.-309C > T). RESULTS: We have performed expression studies in neuronal cell line...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Neurosci Lett
Hlavní autoři: Sleiman, P.M.A., Healy, D.G., Muqit, M.M.K., Yang, Y.X., Van Der Brug, M., Holton, J.L., Revesz, T., Quinn, N.P., Bhatia, K., Diss, J.K.J., Lees, A.J., Cookson, M.R., Latchman, D.S., Wood, N.W.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2009
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4763922/
https://ncbi.nlm.nih.gov/pubmed/19429166
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2009.03.021
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky