Fragile X syndrome disrupts the production of a protein needed for our brain development - and is triggered by an abnormal ...

What is Fragile X syndrome and how do you know if you carry it? - Approximately 1 in 250 women are carriers of the abnormal ...

Fragile X syndrome is caused by a genetic mutation that disrupts brain development, and one in 250 women are carriers, while ...

Mr Richardson explains: "Fragile X Syndrome (FXS) is the most common inherited cause of learning disability. The condition ...

According to the Fragile X Society, patients who suspect they may carry the gene can ask medical professionals for a Fragile ...

According to the Fragile X Society, patients who suspect they may carry the gene can ask medical professionals for a Fragile ...

The Fragile X Society has advised that if patients suspect they might be carriers of the gene, they should request a Fragile ...

Marvel Biosciences Corp. (TSXV: MRVL) (OTCQB: MBCOF), and its wholly owned subsidiary, Marvel Biotechnology Inc.

FXS is a genetic disorder caused by an alteration in the FMR1 gene. It involves a deficiency in FMRP, a protein essential for neural (brain) development. FXS is a leading cause of inherited ...

The FREE methylation test has been closely related to FMR1 protein expression and identified fragile X syndrome (FXS)-affected males and females with 100% specificity in our small study (75 male ...

Italian startup Aptadir has launched with $1.6M to develop drugs targeting DNA hypermethylation for cancer and genetic ...

We identified methylated tandem repeat expansions that resemble the FMR1 CGG repeat that causes fragile X syndrome and investigated their association with traits in the UK Biobank. AFF3 expansion ...