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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Vydáno v:Ann Neurol
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2018
Témata:
Research Articles
On-line přístup: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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