Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype

OBJECTIVE: The basis for clinical variation related to underlying progressive supranuclear palsy (PSP) pathology is unknown. We performed a genome‐wide association study (GWAS) to identify genetic determinants of PSP phenotype. METHODS: Two independent pathological and clinically diagnosed PSP cohor...

Descripción completa

Detalles Bibliográficos
Autores principales: Jabbari, Edwin, Woodside, John, Tan, Manuela M. X., Shoai, Maryam, Pittman, Alan, Ferrari, Raffaele, Mok, Kin Y., Zhang, David, Reynolds, Regina H., de Silva, Rohan, Grimm, Max‐Joseph, Respondek, Gesine, Müller, Ulrich, Al‐Sarraj, Safa, Gentleman, Stephen M., Lees, Andrew J., Warner, Thomas T., Hardy, John, Revesz, Tamas, Höglinger, Günter U., Holton, Janice L., Ryten, Mina, Morris, Huw R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221133/
https://www.ncbi.nlm.nih.gov/pubmed/30066433
http://dx.doi.org/10.1002/ana.25308

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221133/
https://www.ncbi.nlm.nih.gov/pubmed/30066433
http://dx.doi.org/10.1002/ana.25308

Ejemplares similares