{"version":"1.0","provider_name":"JMG Contact blog","provider_url":"https:\/\/blogs.bmj.com\/jmg","author_name":"hqqu","author_url":"https:\/\/blogs.bmj.com\/jmg\/author\/hqiqu\/","title":"ARHGDIA: a novel gene implicated in nephrotic syndrome (Contributed by Dr. Indra Gupta) - JMG Contact blog","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"9Uk7niuaXD\"><a href=\"https:\/\/blogs.bmj.com\/jmg\/2013\/02\/22\/arhgdia-a-novel-gene-implicated-in-nephrotic-syndrome\/\">ARHGDIA: a novel gene implicated in nephrotic syndrome (Contributed by Dr. Indra Gupta)<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/blogs.bmj.com\/jmg\/2013\/02\/22\/arhgdia-a-novel-gene-implicated-in-nephrotic-syndrome\/embed\/#?secret=9Uk7niuaXD\" width=\"600\" height=\"338\" title=\"&#8220;ARHGDIA: a novel gene implicated in nephrotic syndrome (Contributed by Dr. Indra Gupta)&#8221; &#8212; JMG Contact blog\" data-secret=\"9Uk7niuaXD\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\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:\/\/blogs.bmj.com\/jmg\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","description":"Congenital nephrotic syndrome is a rare kidney disease in which affected infants lose protein in the urine and eventually develop kidney failure.\u00a0 Most cases are due to mutations in one of five genes.\u00a0 We have identified a mutation in a new gene, ARHGDIA, encoding Rho GDP dissociation inhibitor alpha (RhoGDIa) that is responsible for this [...]Read More..."}