{"id":1677,"date":"2016-10-20T09:39:00","date_gmt":"2016-10-20T16:39:00","guid":{"rendered":"https:\/\/info.pediatricsdirectory.com\/?p=1677"},"modified":"2023-08-27T00:32:40","modified_gmt":"2023-08-27T04:32:40","slug":"1677-2","status":"publish","type":"post","link":"https:\/\/pediatricscommunity.com\/info\/1677\/","title":{"rendered":""},"content":{"rendered":"\n<div class=\"iframely-embed\"><div class=\"iframely-responsive\" style=\"padding-bottom: 62.45%; padding-top: 120px;\"><a href=\"https:\/\/www.nature.com\/articles\/nrdp201681\" data-iframely-url=\"\/\/cdn.iframe.ly\/api\/iframe?url=https%3A%2F%2Fwww.nature.com%2Farticles%2Fnrdp201681&#038;key=13076e8bfaec4bc8750fefa8568d8747\"><\/a><\/div><\/div><script async src=\"\/\/cdn.iframe.ly\/embed.js\" charset=\"utf-8\"><\/script>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" loading=\"lazy\" width=\"853\" height=\"241\" src=\"https:\/\/pediatricscommunity.com\/info\/wp-content\/uploads\/2023\/08\/mitochondria.png\" alt=\"\" class=\"wp-image-5636\" srcset=\"https:\/\/pediatricscommunity.com\/info\/wp-content\/uploads\/2023\/08\/mitochondria.png 853w, https:\/\/pediatricscommunity.com\/info\/wp-content\/uploads\/2023\/08\/mitochondria-300x85.png 300w, https:\/\/pediatricscommunity.com\/info\/wp-content\/uploads\/2023\/08\/mitochondria-768x217.png 768w\" sizes=\"(max-width: 853px) 100vw, 853px\" \/><\/figure>\n\n\n\n<p><span class=\"standout\">Mitochondrial diseases.<\/span> Genetic disorders are caused by mutations in the genes in mitochondrial and nuclear genomes, encoding dysfunctional proteins within the mitochondria, resulting in defective oxidative phosphorylation, deficits in essential enzyme intermediates, and the accumulation of toxic compounds.<\/p>\n<span class=\"tags-links\"><a href=\"https:\/\/pediatricscommunity.com\/info\/mitochondria\/\" rel=\"tag\">mitochondria<\/a><\/span>","protected":false},"excerpt":{"rendered":"<p>Mitochondrial diseases. Genetic disorders are caused by mutations in the genes in mitochondrial and nuclear genomes, encoding dysfunctional proteins within the mitochondria, resulting in defective oxidative phosphorylation, deficits in essential enzyme intermediates, and the accumulation of toxic compounds. mitochondria<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false},"categories":[252],"tags":[1455],"_links":{"self":[{"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/posts\/1677"}],"collection":[{"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/comments?post=1677"}],"version-history":[{"count":2,"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/posts\/1677\/revisions"}],"predecessor-version":[{"id":5638,"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/posts\/1677\/revisions\/5638"}],"wp:attachment":[{"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/media?parent=1677"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/categories?post=1677"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/pediatricscommunity.com\/info\/wp-json\/wp\/v2\/tags?post=1677"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}