New registry to accelerate research on fragile X syndrome
Wednesday, October 6, 2010 - 05:01
in Health & Medicine
(PhysOrg.com) -- As researchers delve further into the genetic basis for disease, they face a conundrum: finding enough affected people who can fill out a true picture of mutations that can vary from one person to another. A case in point is fragile X syndrome, a genetic mutation that affects approximately one infant boy in 3,600 births, and one infant girl in 4,000-6,000 births.