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Stem Cell Research Produces A Key Discovery For Fragile X Syndrome
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http://www.medicalnewstoday.com/articles/82070.php
Submitted by graymatter 12 months, 15 hours ago
n important finding has been made by McMaster researchers about Fragile X Syndrome (FXS), a sex-linked genetic disorder that affects approximately one in 4,000 males and one in 6,000 females. FXS is the most common genetic disorder associated with mental impairment. The affected gene (FMR1) leads to inactivation of the FMR1 gene product, known as the fragile X mental retardation protein (FMRP). Brain development in the absence of this protein leads to cognitive effects, learning and memory problems, attention deficit, hyperactivity and autistic behaviours. Many children go undiagnosed with Fragile X.
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