{"id":3920,"date":"2017-08-26T04:13:09","date_gmt":"2017-08-26T04:13:09","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=3920"},"modified":"2017-08-26T04:13:09","modified_gmt":"2017-08-26T04:13:09","slug":"nuevas-variantes-mutaciones-y-asociaciones-2","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2017\/08\/26\/nuevas-variantes-mutaciones-y-asociaciones-2\/","title":{"rendered":"Nuevas variantes, mutaciones y asociaciones"},"content":{"rendered":"<p style=\"text-align: justify\">&#8211; <a title=\"J Exp Med 2017; DOI: 10.1084\/jem.20160875 \" href=\"http:\/\/jem.rupress.org\/content\/early\/2017\/07\/18\/jem.20160875?papetoc\" target=\"_blank\">Human venous valve disease caused by mutations in FOXC2 and GJC2<\/a><br \/>\n&#8211; <a title=\"J Exp Med 2017; DOI: 10.1084\/jem.20161810 \" href=\"http:\/\/jem.rupress.org\/content\/early\/2017\/07\/26\/jem.20161810?papetoc\" target=\"_blank\">A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis<\/a><br \/>\n&#8211; <a title=\"Nature Genetics 2017;49:1255\u20131260. \" href=\"http:\/\/www.nature.com\/ng\/journal\/v49\/n8\/full\/ng.3895.html\" target=\"_blank\">Variants in the fetal genome near FLT1 are associated with risk of preeclampsia<\/a><br \/>\n&#8211; <a title=\"Journal of Human Genetics 2017;62:797\u2013801; \" href=\"http:\/\/www.nature.com\/jhg\/journal\/v62\/n8\/full\/jhg201738a.html\" target=\"_blank\">Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia<\/a><br \/>\n&#8211; <a title=\"Nature Genetics 2017;49:1182\u20131191.\" href=\"http:\/\/www.nature.com\/ng\/journal\/v49\/n8\/full\/ng.3897.html\" target=\"_blank\">Identification of sequence variants influencing immunoglobulin levels<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Human venous valve disease caused by mutations in FOXC2 and GJC2 &#8211; A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis &#8211; Variants in the fetal genome near FLT1 are associated with risk of preeclampsia &#8211; Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia &#8211; Identification [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[15,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3920"}],"collection":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/users\/125"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/comments?post=3920"}],"version-history":[{"count":1,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3920\/revisions"}],"predecessor-version":[{"id":3921,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3920\/revisions\/3921"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=3920"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=3920"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=3920"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}