{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,11]],"date-time":"2026-05-11T06:10:23Z","timestamp":1778479823579,"version":"3.51.4"},"reference-count":66,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2025,12,30]],"date-time":"2025-12-30T00:00:00Z","timestamp":1767052800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"funder":[{"DOI":"10.13039\/501100001732","name":"Danish National Research Foundation","doi-asserted-by":"publisher","award":["10.46540\/2032-00333B"],"award-info":[{"award-number":["10.46540\/2032-00333B"]}],"id":[{"id":"10.13039\/501100001732","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100009708","name":"Novo Nordisk Foundation","doi-asserted-by":"publisher","award":["NNF23OC0081817"],"award-info":[{"award-number":["NNF23OC0081817"]}],"id":[{"id":"10.13039\/501100009708","id-type":"DOI","asserted-by":"publisher"}]},{"name":"National Institute of Neurological Disorders and Stroke of the National Institutes of Health","award":["U54NS108251"],"award-info":[{"award-number":["U54NS108251"]}]},{"name":"National Institute of Neurological Disorders and Stroke of the National Institutes of Health","award":["U01HG007672"],"award-info":[{"award-number":["U01HG007672"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,2,10]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Calmodulin is an intracellular Ca2+ sensor that regulates numerous cellular processes through binding effector proteins and changing their activity. Humans have three calmodulin paralogs, CALM1, CALM2 and CALM3, encoding identical proteins, and missense variants in all three are included in the ACMG recommendations for reporting of secondary findings related to early onset sudden cardiac death caused by arrhythmias long QT syndrome and CPVT. Recently, a subset of individuals with de novo variants in calmodulin genes were described who also presented with neurologic phenotypes. Here we report two individuals with the same de novo variant c.419A\u2009&amp;gt;\u2009T in CALM1 or CALM2 that may generate a 5\u2032 splice donor gain and\/or a missense change p.E140V. These individuals share hypotonia, motor delay, intellectual disability, and abnormal electroencephalograms but lack cardiac arrhythmia\/electrocardiogram abnormalities of previously described CALM-associated disease, suggesting the variant causes phenotypic expansion beyond the known Mendelian phenotypes. RNA-seq of the CALM1 proband blood\u2019s sample revealed that most transcripts from the variant allele showed usage of the new splice site or intron retention, without NMD, resulting in frameshifted C-terminal truncations, while a minority resulted in production of the p.E140V missense protein. We modeled the CALM1\/2 p.E140V variant as well as a known arrhythmia variant, CALM1 p.E141G, using the C. elegans ortholog cmd-1. We found that cmd-1 E140V displayed both qualitative and quantitative differences in phenotype from E141G, indicating distinct genetic mechanisms. Together, these findings support CALM1\/2 phenotypic expansion, with c.419A\u2009&amp;gt;\u2009T p.E140V resulting in neurologic, but not arrhythmia phenotypes.<\/jats:p>","DOI":"10.1093\/hmg\/ddaf195","type":"journal-article","created":{"date-parts":[[2025,12,19]],"date-time":"2025-12-19T13:03:50Z","timestamp":1766149430000},"source":"Crossref","is-referenced-by-count":0,"title":["Phenotypic expansion of\n                    <i>CALM1\/2<\/i>\n                    -associated disorders to include neurologic phenotypes without arrhythmia"],"prefix":"10.1093","volume":"35","author":[{"given":"Hieu D","family":"Hoang","sequence":"first","affiliation":[{"name":"Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine , 660 South Euclid Avenue, St. Louis, MO 63110 ,","place":["United States"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rebecca C","family":"Spillmann","sequence":"additional","affiliation":[{"name":"Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine , 905 Lasalle Street, Durham, NC 27710 ,","place":["United States"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniel J","family":"Wegner","sequence":"additional","affiliation":[{"name":"Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine , 660 South Euclid Avenue, St. Louis, MO 63110 ,","place":["United States"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria G","family":"Tedesco","sequence":"additional","affiliation":[{"name":"Medical Genetics and Rare Diseases Unit, Maternal-Infantile Department, Hospital of Perugia , Piazzale Menghini 8\/9, 06129 Perugia ,","place":["Italy"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9247-8551","authenticated-orcid":false,"given":"Malene","family":"Brohus","sequence":"additional","affiliation":[{"name":"Department of Chemistry and Bioscience, Aalborg University , Fredrik Bajers Vej 7H, 9220 Aalborg ,","place":["Denmark"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antonio","family":"Novelli","sequence":"additional","affiliation":[{"name":"Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Ges\u00f9 Children's Hospital, IRCCS , Viale San Paolo 15, 00146 Rome ,","place":["Italy"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fabrizia","family":"Stregapede","sequence":"additional","affiliation":[{"name":"Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Ges\u00f9 Children's Hospital, IRCCS , Viale San Paolo 15, 00146 Rome ,","place":["Italy"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniela","family":"Rogaia","sequence":"additional","affiliation":[{"name":"Medical Genetics and Rare Diseases Unit, Maternal-Infantile Department, Hospital of Perugia , Piazzale Menghini 8\/9, 06129 Perugia 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63110 ,","place":["United States"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Suk","family":"Regmi","sequence":"additional","affiliation":[{"name":"Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine , 660 South Euclid Avenue, St. Louis, MO 63110 ,","place":["United States"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Miryam R S","family":"Foti","sequence":"additional","affiliation":[{"name":"Genetics Unit, Medical Science and Maternal-Infantile Department, Hospital Sant'Anna of Ferrara , Via Fossato di Mortara, 74, 44121 Ferrara ,","place":["Italy"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dustin","family":"Baldridge","sequence":"additional","affiliation":[{"name":"Edward Mallinckrodt Department of Pediatrics, Washington University in St. Louis School of Medicine , 660 South Euclid Avenue, St. Louis, MO 63110 ,","place":["United 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