{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T15:53:52Z","timestamp":1791302032183,"version":"4.1.0"},"reference-count":50,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T00:00:00Z","timestamp":1780876800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T00:00:00Z","timestamp":1780876800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Annals of Neurology"],"published-print":{"date-parts":[[2026,9]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      Biallelic variants in genes encoding the RNA polymerase III complex (Pol III) cause a spectrum of neurological disorders primarily affecting the central nervous system. Monoallelic variants have been reported in the\n                      <jats:italic>POLR3B<\/jats:italic>\n                      subunit only, associated with neurodevelopmental disorder, epilepsy, and peripheral neuropathy. We describe a novel Pol III\u2010related disorder caused by monoallelic variants in\n                      <jats:italic>POLR3A<\/jats:italic>\n                      and presenting primarily with peripheral neuropathy.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We performed clinical and genetic investigation of the affected families. Biophysical characterization of mutant proteins was performed in silico. Immunoblotting, interactomics, and transcriptomics characterization were done in cellular models.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      We identified 11 patients across 8 unrelated families harboring heterozygous missense variants in\n                      <jats:italic>POLR3A,<\/jats:italic>\n                      occurring de novo or segregating in an autosomal\u2010dominant fashion. The patients presented with an early\u2010onset, progressive sensorimotor peripheral polyneuropathy with intermediate to demyelinating ranges of nerve conduction slowing, occasionally accompanied with neurological or non\u2010neurological features. White matter abnormalities, characteristic for the biallelic Pol III\u2010related disorders, where not observed in the brain magnetic resonance imaging (MRI) evaluations. The neuropathy\u2010associated variants cluster in regions critical for Pol III activity. We observed mis\u2010regulation of individual Pol III targets and global downregulation of tRNA pools in patient\u2010derived cells. This Pol III dysfunction was not due to impaired POLR3A expression, subcellular localization, or subunit interactions.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interpretation<\/jats:title>\n                    <jats:p>\n                      Our findings expand the Pol III\u2010related disease spectrum beyond the known biallelic phenotypes and establish\n                      <jats:italic>POLR3A<\/jats:italic>\n                      as a novel peripheral neuropathy\u2010associated gene. This work highlights a central role of Pol III dysfunction in disease and reinforces the link between tRNA metabolism and peripheral neurodegeneration. ANN NEUROL 2026;100:655\u2013671\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/ana.78268","type":"journal-article","created":{"date-parts":[[2026,6,9]],"date-time":"2026-06-09T04:51:16Z","timestamp":1780980676000},"page":"655-671","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Monoallelic\n                    <scp>\n                      <i>POLR3A<\/i>\n                    <\/scp>\n                    Variants Cause Early\u2010Onset Peripheral Neuropathy"],"prefix":"10.1002","volume":"100","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1668-1683","authenticated-orcid":false,"given":"Luiza L. 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