{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,24]],"date-time":"2026-08-24T13:25:55Z","timestamp":1787577955867,"version":"build-2736575974"},"reference-count":8,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2020,1,1]],"date-time":"2020-01-01T00:00:00Z","timestamp":1577836800000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000871","name":"Mayo Clinic","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000871","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Child Neurology Open"],"published-print":{"date-parts":[[2020,1,1]]},"abstract":"<jats:p>Variants in PURA have recently been associated with an autosomal dominant form of PURA-related neurodevelopmental disorders. Using whole exome sequencing, patients with neurological phenotypes including hypotonia, developmental delay, learning disabilities, and seizures were identified to have de novo variants in PURA. We describe a proband with features similar to the previously described cases with PURA variants, but including additional features, such as short stature, delayed bone age, and delayed puberty. Exome sequencing revealed a novel pathogenic nonsense variant, c.190A&gt;T (p.Lys64*; NM_005859), in PURA that was not inherited from the proband\u2019s mother. In the recent literature, a significant number of patients with variants in PURA have been described, but to our knowledge, none of these patients have the delayed bone age and growth plateau observed in the proband. It is therefore possible that the above PURA variant may be responsible for the novel features and thus expands the PURA-related phenotype spectrum.<\/jats:p>","DOI":"10.1177\/2329048x20955003","type":"journal-article","created":{"date-parts":[[2020,10,14]],"date-time":"2020-10-14T07:13:51Z","timestamp":1602659631000},"page":"2329048X2095500","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":6,"title":["Expansion of\n                    <i>PURA<\/i>\n                    -Related Phenotypes and Discovery of a Novel PURA Variant: A Case Report"],"prefix":"10.1177","volume":"7","author":[{"given":"Nicole J.","family":"Boczek","sequence":"first","affiliation":[{"name":"Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8324-506X","authenticated-orcid":false,"given":"Erica L.","family":"Macke","sequence":"additional","affiliation":[{"name":"Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer","family":"Kemppainen","sequence":"additional","affiliation":[{"name":"Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eric W.","family":"Klee","sequence":"additional","affiliation":[{"name":"Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Biomedical Informatics, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3373-6260","authenticated-orcid":false,"given":"Deborah L.","family":"Renaud","sequence":"additional","affiliation":[{"name":"Department of Neurology, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Pediatrics, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ralitza H.","family":"Gavrilova","sequence":"additional","affiliation":[{"name":"Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA"},{"name":"Department of Neurology, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2020,10,14]]},"reference":[{"key":"bibr1-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.38521"},{"key":"bibr2-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1016\/j.ymgme.2017.12.436"},{"key":"bibr3-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmg.2018.06.010"},{"key":"bibr4-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1136\/jmedgenet-2014-102798"},{"key":"bibr5-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2014.09.014"},{"key":"bibr6-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1136\/jmedgenet-2017-104946"},{"key":"bibr7-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1101\/mcs.a000356"},{"key":"bibr8-2329048X20955003","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.35439"}],"container-title":["Child Neurology Open"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/2329048X20955003","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/journals.sagepub.com\/doi\/full-xml\/10.1177\/2329048X20955003","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/2329048X20955003","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,28]],"date-time":"2026-04-28T15:58:01Z","timestamp":1777391881000},"score":1,"resource":{"primary":{"URL":"http:\/\/journals.sagepub.com\/doi\/10.1177\/2329048X20955003"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,1,1]]},"references-count":8,"alternative-id":["10.1177\/2329048X20955003"],"URL":"https:\/\/doi.org\/10.1177\/2329048x20955003","relation":{},"ISSN":["2329-048X","2329-048X"],"issn-type":[{"value":"2329-048X","type":"print"},{"value":"2329-048X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2020,1,1]]}}}