Male and female donors 18–68 years of age with no known history of neuropsychiatric or neurological conditions (‘control’ cases) were considered for inclusion in this study (Extended Data Table 1). Routine serological screening for infectious disease (HIV, hepatitis B and hepatitis C) was conducted using donor blood samples, and only those donors who were negative for all three tests were considered for inclusion. Only those specimens with RNA integrity (RIN) values of 7.0 or more were considered for inclusion. Postmortem brain specimens were processed as described3 (link). Briefly, coronal brain slabs were cut at 1 cm intervals and frozen for storage at −80 °C until further use. Putative hand and trunk-lower limb regions of the primary motor cortex were identified, removed from slabs of interest, and subdivided into smaller blocks. One block from each donor was processed for cryosectioning and fluorescent Nissl staining (Neurotrace 500/525, ThermoFisher Scientific). Stained sections were screened for histological hallmarks of primary motor cortex. After verifying that regions of interest contained M1, blocks were processed for nucleus isolation as described below.
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