{"version":"1.0","provider_name":"Centro Andaluz Alfa-1","provider_url":"https:\/\/centroandaluzalfa1.org\/en\/","title":"Alpha 1 deficiency as a hereditary disease - Centro Andaluz Alfa-1","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"iV3qTsSWjS\"><a href=\"https:\/\/centroandaluzalfa1.org\/en\/alpha-1-deficiency-as-a-hereditary-disease\/\">Alpha 1 deficiency as a hereditary disease<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/centroandaluzalfa1.org\/en\/alpha-1-deficiency-as-a-hereditary-disease\/embed\/#?secret=iV3qTsSWjS\" width=\"600\" height=\"338\" title=\"&#8220;Alpha 1 deficiency as a hereditary disease&#8221; &#8212; Centro Andaluz Alfa-1\" data-secret=\"iV3qTsSWjS\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/centroandaluzalfa1.org\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","thumbnail_url":"https:\/\/centroandaluzalfa1.org\/wp-content\/uploads\/2019\/10\/research.png","thumbnail_width":737,"thumbnail_height":313,"description":"The AAT gene consists of two alleles, which are passed from parent to child by inheritance. Each child receives an allele from each of its parents. Normal alleles, present in 85-90% of individuals, are called M, and therefore a normal individual receives two M alleles (one from each parent), which form an MM genotype."}