{"id":1431075,"date":"2020-10-16T11:36:27","date_gmt":"2020-10-16T09:36:27","guid":{"rendered":"https:\/\/staging-wp-int.laboklin.com\/products\/genetics\/hereditary-diseases\/cat\/head-defect\/"},"modified":"2022-11-22T12:10:29","modified_gmt":"2022-11-22T11:10:29","slug":"head-defect","status":"publish","type":"page","link":"https:\/\/laboklin.com\/no\/products\/genetics\/hereditary-diseases\/cat\/head-defect\/","title":{"rendered":"Head defect"},"content":{"rendered":"<h3 class=\"csc-firstHeader\">Head defect<\/h3><p><span>LABOKLIN Service ID: 8465<\/span><\/p><p class=\"bodytext\">A recessive mutation that causes a congenital craniofacial defect in Burmese cats has been discovered by the Lyons Feline Genetics Research Laboratory at UC Davis. The mutation affects function of a gene significant for facial development. The Burmese Head Defect mutation is common in the Contemporary lines of Burmese in the United States. One copy of the mutation does not cause the craniofacial defect but may produce a shortened facial structure (brachycephaly). Cats with two copies of the mutation have the severe craniofacial defect that is incompatible with life. <\/p><table class=\"tx-laboklinleistung-table contenttable contenttable-2\" style=\"margin-top: 35px;\"><tr><td class=\"td-0\"><strong>Method<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">FLP<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Breed list<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">Burmese<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Heredity<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">autosomal recessive<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Duration<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">1 - 2 weeks after arrival of the sample in the lab<\/p><\/td><\/tr><\/table>\n","protected":false},"excerpt":{"rendered":"<p>Head defectLABOKLIN Service ID: 8465A recessive mutation that causes a congenital craniofacial defect in Burmese cats has been discovered by the Lyons Feline Genetics Research Laboratory at UC Davis. The mutation affects function of a gene significant for facial development. The Burmese Head Defect mutation is common in the Contemporary lines of Burmese in the&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1421755,"menu_order":29,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","footnotes":""},"class_list":["post-1431075","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/pages\/1431075","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/comments?post=1431075"}],"version-history":[{"count":0,"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/pages\/1431075\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/pages\/1421755"}],"wp:attachment":[{"href":"https:\/\/laboklin.com\/no\/wp-json\/wp\/v2\/media?parent=1431075"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}