Year: 2026
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Correction of the molecular phenotype of X-linked Dystonia-Parkinsonism reveals a non-canonical function of BRD4
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Regional and Compartmental Changes Drive Progressive Patterns of Striatal Degeneration in X-Linked Dystonia Parkinsonism
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Therapeutic targeting of alternative splicing caused by a lethal noncoding structural variant in X-linked dystonia parkinsonism
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Genome writing to dissect consequences of SVA retrotransposon disease X-Linked Dystonia Parkinsonism
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Myelin pathology is a key feature of X-linked Dystonia Parkinsonism
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MSH3 is a genetic modifier of somatic repeat instability in X-linked dystonia parkinsonism
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Biostatistical analysis of X-Linked Dystonia-Parkinsonism
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Using mosaicism to recognize core pathogenic processes in XDP
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Understand Tau Pathology in XDP Patients
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Defining TAF1 Regulatory Networks and Isoform-Specific Interactomes in XDP