Merry Christmas and happy new year!

MGM

The first pediatric case of glucagon receptor defect...

The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine. Hong Li, Lihua Zhao, Rani Singh, J. Nina Ham, Doris O. Fadoju, Lora J. H. Bean, Yan Zhang, Yong Xu, H. Eric Xu, Michael J. Gambello Molecular Genetics …

Funding

Funding Opportunities (19/12/2018)

Spring 2019 Project Grant Competition (CIHR, Canada) The Canadian Institutes for Health Research has launched its spring funding opportunity. This announcement is desinged to capture ideas with the greatest potential to advance health-related fundamental or applied knowledge, health research, …

UPCOMING EVENTS (19/12/2018)

Global Commission to End the Diagnostic Odyssey of Children with Rare Diseases On Wednesday, February 20, 2019, there will be the official launch of the Global Commission to End the Diagnostic Odyssey of Children with a Rare Disease's ("The Global Commission") digital roadmap for shortening the …

Patient's Box

Patient organizations becoming members of the UDNI. We are excited to announce the opportunity for patient organizations around the world to officially join the Undiagnosed Disease Network International (UDNI) as members! The UDNI represents one of the most exciting international initiatives for …