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The aim of this study was to characterise the genetic profile of IRD patients in Korea using WES.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We performed comprehensive molecular testing in 168 unrelated Korean IRD patients using WES. The potential pathogenicity of candidate variants was assessed using the American College of Medical Genetics and Genomics and the Association for Molecular Pathology variant interpretation guidelines, in silico prediction tools, published literature, and compatibility with known phenotypes or inheritance patterns.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Causative variants were detected in 86\/168 (51.2%) IRD patients, including 58\/107 (54.2%) with retinitis pigmentosa, 7\/15 (46.7%) with cone and cone-rod dystrophy, 2\/3 (66.6%) with Usher syndrome, 1\/2 (50.0%) with congenital stationary night blindness, 2\/2 (100.0%) with Leber congenital amaurosis, 1\/1 (100.0%) with Bietti crystalline dystrophy, 1\/1 (100.0%) with Joubert syndrome, 9\/10 (90.0%) with Stargardt macular dystrophy, 1\/10 (10.0%) with vitelliform macular dystrophy, 1\/11 (9.1%) with other forms of macular dystrophy, and 3\/4 (75.0%) with choroideraemia.\n                      <jats:italic>USH2A<\/jats:italic>\n                      ,\n                      <jats:italic>ABCA4<\/jats:italic>\n                      , and\n                      <jats:italic>EYS<\/jats:italic>\n                      were the most common causative genes associated with IRD. For retinitis pigmentosa, variants of\n                      <jats:italic>USH2A<\/jats:italic>\n                      and\n                      <jats:italic>EYS<\/jats:italic>\n                      were the most common causative gene mutations.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>This study demonstrated the distribution of causative genetic mutations in Korean IRD patients. The data will serve as a reference for future genetic screening and development of treatment modalities for Korean IRD patients.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1186\/s12920-021-00874-6","type":"journal-article","created":{"date-parts":[[2021,3,10]],"date-time":"2021-03-10T02:03:20Z","timestamp":1615341800000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":58,"title":["Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration"],"prefix":"10.1186","volume":"14","author":[{"given":"Dae Joong","family":"Ma","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hyun-Seob","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kwangsoo","family":"Kim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Seongmin","family":"Choi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Insoon","family":"Jang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Seo-Ho","family":"Cho","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chang Ki","family":"Yoon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eun Kyoung","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1795-202X","authenticated-orcid":false,"given":"Hyeong Gon","family":"Yu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2021,3,10]]},"reference":[{"key":"874_CR1","doi-asserted-by":"publisher","first-page":"107","DOI":"10.1016\/j.preteyeres.2017.10.004","volume":"63","author":"MF Dias","year":"2018","unstructured":"Dias MF, Joo K, Kemp JA, Fialho SL, da Silva Cunha A Jr, Woo SJ, et al. 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