rosenblatt /newsroom/taxonomy/term/10135/all en Epigenetic alteration of a vitamin B12 processing gene shines new light on our understanding of rare diseases /newsroom/channels/news/epigenetic-alteration-vitamin-b12-processing-gene-shines-new-light-our-understanding-rare-diseases-284319 <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 黑料不打烊 University and the Research Institute of the 黑料不打烊 University 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> Tue, 30 Jan 2018 19:16:41 +0000 laurie.devine@mcgill.ca 32909 at /newsroom