{"id":595,"date":"2026-03-02T11:58:14","date_gmt":"2026-03-02T10:58:14","guid":{"rendered":"https:\/\/dev.genocan.eu\/test\/trpaslictvi\/"},"modified":"2026-05-23T23:33:16","modified_gmt":"2026-05-23T21:33:16","slug":"trpaslictvi","status":"publish","type":"test","link":"https:\/\/dev.genocan.eu\/en\/test\/trpaslictvi\/","title":{"rendered":"Dwarfism"},"content":{"rendered":"<p>Dwarfism is an autosomal recessive disease, so the disease affects individuals who receive a mutated gene from both parents.<\/p>\n<p>The disease is caused by a deletion of the 7 bp repeat in intron 5 of the LHX3 gene, in one German Shepherd the insertion of the trinucleotide sequence ACA in exon 5 of the same gene was observed.<\/p>\n<p>GenoCan detects both mutations leading to a dwarfism.<\/p>\n","protected":false},"template":"","breed":[132,114,122],"class_list":["post-595","test","type-test","status-publish","hentry","breed-czechoslovakian-wolfdog","breed-german-shepherd","breed-saarloos-wolfdog"],"acf":[],"_links":{"self":[{"href":"https:\/\/dev.genocan.eu\/en\/wp-json\/wp\/v2\/test\/595","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/dev.genocan.eu\/en\/wp-json\/wp\/v2\/test"}],"about":[{"href":"https:\/\/dev.genocan.eu\/en\/wp-json\/wp\/v2\/types\/test"}],"wp:attachment":[{"href":"https:\/\/dev.genocan.eu\/en\/wp-json\/wp\/v2\/media?parent=595"}],"wp:term":[{"taxonomy":"breed","embeddable":true,"href":"https:\/\/dev.genocan.eu\/en\/wp-json\/wp\/v2\/breed?post=595"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}