1.0Gene Therapy Center/genetherapyBradley Olson/genetherapy/author/bradley-olson/rich600338<blockquote class="wp-embedded-content" data-secret="CquQ5MASi7"><a href="/genetherapy/directory/peirong-hu/">Peirong Hu</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="/genetherapy/directory/peirong-hu/embed/#?secret=CquQ5MASi7" width="600" height="338" title="“Peirong Hu” — Gene Therapy Center" data-secret="CquQ5MASi7" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript"> /* <![CDATA[ */ /*! 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); /* ]]> */ </script> /genetherapy/wp-content/uploads/sites/811/2018/10/peirong-hu.jpeg150150Research Interests Krabbe disease is a lysosomal storage disorder caused by GALC (galactocerebrosidase) mutation. According to the onset time and severity, it can be divided into the infantile type, juveniletype and adult type. Patients showed progressive demyelination, severe gliosis, the presence of globoid cells, and destruction of brain cells. Hematopoietic stem cell transplantation has been … Read more