17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes

BACKGROUND: Parkinson’s disease (PD) is genetically associated with the H1 haplotype of the MAPT 17q.21.31 locus, although the causal gene and variants underlying this association have not been identified. METHODS: To better understand the genetic contribution of this region to PD and to identify no...

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Detalles Bibliográficos
Autores principales: Bowles, Kathryn R., Pugh, Derian A., Liu, Yiyuan, Patel, Tulsi, Renton, Alan E., Bandres-Ciga, Sara, Gan-Or, Ziv, Heutink, Peter, Siitonen, Ari, Bertelsen, Sarah, Cherry, Jonathan D., Karch, Celeste M., Frucht, Steven J., Kopell, Brian H., Peter, Inga, Park, Y. J., Charney, Alexander, Raj, Towfique, Crary, John F., Goate, A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284779/
https://www.ncbi.nlm.nih.gov/pubmed/35841044
http://dx.doi.org/10.1186/s13024-022-00551-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284779/
https://www.ncbi.nlm.nih.gov/pubmed/35841044
http://dx.doi.org/10.1186/s13024-022-00551-x

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