/channels/news_feeds/all/term/rosenblatt/rss en /channels/channels/news/epigenetic-alteration-vitamin-b12-processing-gene-shines-new-light-our-understanding-rare-diseases-284319 <div class="field field-name-body field-type-text-with-summary field-label-hidden"><div class="field-items"><div class="field-item even"><p>Rare hereditary recessive diseases were thought to be expressed in offspring only when both parents carry a mutation in the causal gene, but a new study is changing this paradigm. An international research team led by scientists at the University of Lorraine in France along with 9I制作厂免费 and the Research Institute of the 9I制作厂免费 Health Centre (RI-MUHC) in Canada discovered a new cause of a rare condition known as<em> cblC</em>, that they named 鈥渆pi-<em>cblC</em>鈥�. They reported it in patients from Europe and the United States.</p></div></div></div><div class="field field-name-field-primary-image field-type-image field-label-hidden"><div class="field-items"><div class="field-item even"><img class="no-float" src="/channels/files/channels/styles/wysiwyg_medium/public/channels/image/rosenblatt_bonne_photo.jpg?itok=Yw1ewXdS" width="160" height="106" alt="" /></div></div></div><div class="field field-name-field-published-date field-type-datestamp field-label-hidden"><div class="field-items"><div class="field-item even"><div class="custom-multi-date"><div class="multi-date first"><span class="label">Published: </span><span class="day">30 </span><span class="month">January </span><span class="year">2018</span></div></div></div></div></div> Tue, 30 Jan 2018 19:16:43 +0000 webfull 134593 at /channels