{"id":12147,"date":"2021-09-22T14:51:33","date_gmt":"2021-09-22T12:51:33","guid":{"rendered":"https:\/\/www.humangenetik-umg.de\/?p=12147"},"modified":"2021-09-23T10:08:09","modified_gmt":"2021-09-23T08:08:09","slug":"newly-identified-biallelic-yrdc-variant-causes-developmental-disorder-with-features-of-premature-ageing","status":"publish","type":"post","link":"https:\/\/www.humangenetik-umg.de\/en\/newly-identified-biallelic-yrdc-variant-causes-developmental-disorder-with-features-of-premature-ageing\/","title":{"rendered":"Newly identified biallelic YRDC variant causes developmental disorder with features of premature ageing"},"content":{"rendered":"<div class=\"wpb-content-wrapper\">[vc_row][vc_column][mk_padding_divider][\/vc_column][\/vc_row][vc_row][vc_column][mk_image src=&#8221;https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2021\/09\/yrdc-visual-abstract-en.png&#8221; image_size=&#8221;full&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][mk_padding_divider][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text]<strong>Biallelic variants in YRDC cause a developmental disorder with progeroid features<\/strong><br \/>\nSchmidt J, Goergens J, Pochechueva T, Kotter A, Schwenzer N, Sitte M, Werner G, Altm\u00fcller J, Thiele H, N\u00fcrnberg P, Isensee J, Li Y, M\u00fcller C, Leube B, Reinhardt HC, Hucho T, Salinas G, Helm M, Jachimowicz RD, Wieczorek D, Kohl T, Lehnart SE, Yigit G, Wollnik B.<br \/>\n<em>Hum Genet.<\/em> 2021 Sep 20. doi: 10.1007\/s00439-021-02347-3. Epub ahead of print.<\/p>\n[mk_button dimension=&#8221;flat&#8221; size=&#8221;medium&#8221; icon=&#8221;mk-icon-long-arrow-right&#8221; icon_anim=&#8221;side&#8221; url=&#8221;https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/34545459&#8243; target=&#8221;_blank&#8221; bg_color=&#8221;#006699&#8243; btn_hover_bg=&#8221;#000000&#8243; btn_hover_txt_color=&#8221;#ffffff&#8221;]Article in PubMed[\/mk_button][mk_padding_divider size=&#8221;30&#8243;][\/vc_column_text][\/vc_column][\/vc_row]\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][mk_padding_divider][\/vc_column][\/vc_row][vc_row][vc_column][mk_image src=&#8221;https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2021\/09\/yrdc-visual-abstract-en.png&#8221; image_size=&#8221;full&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][mk_padding_divider][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text]Biallelic variants in YRDC cause a developmental disorder with progeroid features Schmidt J, Goergens J, Pochechueva T, Kotter A, Schwenzer N, Sitte M, Werner G, Altm\u00fcller J, Thiele H, N\u00fcrnberg P, Isensee J, Li Y, M\u00fcller C, Leube B, Reinhardt HC, Hucho T, Salinas G, Helm M, Jachimowicz RD, Wieczorek D, Kohl T, [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[51,52],"tags":[],"class_list":["post-12147","post","type-post","status-publish","format-standard","hentry","category-news","category-research"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - 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