In 2012, four-year-old Bertrand Might became the first-ever patient diagnosed with a rare genetic disorder called N-glycanase (NGLY1) deficiency. Although his life was cut short, his legacy will benefit 亚洲自慰视频ren...
Janice Hanson's journey, which began with the birth of her first 亚洲自慰视频 57 years earlier, culminated with the discovery of a rare genetic mutation responsible for the constellation of symptoms...
A 亚洲自慰视频 of Utah-led initiative to help people with rare and untreatable diseases was highlighted by the White House at the Precision Medicine Initiative Summit today. Patient Empowered Precision Medicine...