Variation at the TRIM11 locus modifies Progressive Supranuclear Palsy phenotype.
Jabbari E, Woodside J, Tan MMX et al.
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Abstract
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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.
130 European ancestry non-Richardson's syndrome cases, 367 European ancestry Richardson's syndrome controls
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