{"id":16520,"date":"2012-11-01T00:00:00","date_gmt":"2012-11-01T04:00:00","guid":{"rendered":"https:\/\/genomequebec.com\/actualites-et-publications\/mutations-in-tmem231-cause-joubert-syndrome-in-french-canadians\/"},"modified":"2012-11-01T00:00:00","modified_gmt":"2012-11-01T04:00:00","slug":"mutations-in-tmem231-cause-joubert-syndrome-in-french-canadians","status":"publish","type":"post","link":"https:\/\/genomequebec.com\/en\/news-and-publications\/mutations-in-tmem231-cause-joubert-syndrome-in-french-canadians\/","title":{"rendered":"Mutations in TMEM231 cause Joubert syndrome in French Canadians"},"content":{"rendered":"<p>The researchers Jacques L. Michaud (CHU Ste-Justine), Jacek Mejewski (Universit\u00e9 McGill) and Guy A. Rouleau (CHU Ste-Justine) have discovered mutations in TMEM231 causing Joubert syndrome, a rare desease in French Canadian population.<\/p>\n<p>Read more in the <a href=\"http:\/\/jmg.bmj.com\/content\/early\/2012\/09\/24\/jmedgenet-2012-101132.full\" target=\"_blank\" rel=\"noopener\">Journal of Medical Genetics<\/a>, October 15, 2012.<\/p>\n<p>\u00a0<\/p>\n<p>The project is part of the FORGE Canada Consortium and the exome sequencing has been done at the McGill University and G\u00e9nome Qu\u00e9bec Innovation Centre.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The researchers Jacques L. Michaud (CHU Ste-Justine), Jacek Mejewski (Universit\u00e9 McGill) and Guy A. Rouleau (CHU Ste-Justine) have discovered mutations in TMEM231 causing Joubert syndrome, a rare desease in French&hellip;<\/p>\n","protected":false},"author":1,"featured_media":15275,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"categories":[294],"tags":[],"class_list":["post-16520","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-nouvelles"],"acf":[],"_links":{"self":[{"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/posts\/16520","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/comments?post=16520"}],"version-history":[{"count":0,"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/posts\/16520\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/media\/15275"}],"wp:attachment":[{"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/media?parent=16520"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/categories?post=16520"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/genomequebec.com\/en\/wp-json\/wp\/v2\/tags?post=16520"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}