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It is typically caused by pathogenic variants within the\n                    <jats:italic>FOXE3<\/jats:italic>\n                    or\n                    <jats:italic>HCCS<\/jats:italic>\n                    genes; however, it can also be associated with\n                    <jats:italic>GJA8<\/jats:italic>\n                    pathogenic variants.\n                    <jats:italic>GJA8<\/jats:italic>\n                    should be included in the genetic testing of patients with this condition.\n                  <\/jats:p>","DOI":"10.1002\/ccr3.70286","type":"journal-article","created":{"date-parts":[[2025,5,6]],"date-time":"2025-05-06T01:25:08Z","timestamp":1746494708000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Congenital Aphakia Associated With a\n                    <scp>\n                      <i>GJA8<\/i>\n                    <\/scp>\n                    Pathogenic Variant: A Case Report"],"prefix":"10.1002","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2832-044X","authenticated-orcid":false,"given":"Sarah A. 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