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Our report adds<jats:italic>TRPM3<\/jats:italic>to the list of Mendelian disease\u2013associated genes that can be associated with CP and provides further evidence for the pathogenicity of the variant p.(Asn1126Asp).<\/jats:p>","DOI":"10.1101\/mcs.a006293","type":"journal-article","created":{"date-parts":[[2023,9,8]],"date-time":"2023-09-08T19:15:11Z","timestamp":1694200511000},"page":"a006293","source":"Crossref","is-referenced-by-count":9,"title":["De novo<i>TRPM3<\/i>missense variant associated with neurodevelopmental delay and manifestations of cerebral palsy"],"prefix":"10.1101","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6670-9157","authenticated-orcid":false,"given":"Jagadish Chandrabose","family":"Sundaramurthi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9118-8798","authenticated-orcid":false,"given":"Anita 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