1.0Research for Rarehttps://www.research4rare.de/en/mroeselehttps://www.research4rare.de/en/author/mroesele/rich600338<blockquote class="wp-embedded-content" data-secret="73LJG9J0O5"><a href="https://www.research4rare.de/en/alumni/pid-net/">PID NET</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://www.research4rare.de/en/alumni/pid-net/embed/#?secret=73LJG9J0O5" width="600" height="338" title="“PID NET” — Research for Rare" data-secret="73LJG9J0O5" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script> /*! This file is auto-generated */ !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); //# sourceURL=https://www.research4rare.de/wp-includes/js/wp-embed.min.js </script> https://www.research4rare.de/wp-content/uploads/2012/12/PIDnet.jpg36086Primary immunodeficiency disorders (PID) represent rare inborn errors of the immune system predisposing to recurrent infections, autoimmunity, allergy, and cancer. Identifying underlying genetic causes and the pathophysiological basis of these rare diseases is not only important for the development of innovative gene-based therapeutic strategies, but has wide implications for understanding many of the more common […]