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...

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Detalhes bibliográficos
Publicado no:Ann Neurol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6221133/
https://ncbi.nlm.nih.gov/pubmed/30066433
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.25308
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