FMRP
Quick Summary
FMRP, or fragile-X mental retardation protein, is a protein crucial for brain development and synapse maturation. The symptoms of fragile-X syndrome, a chromosomal disorder causing intellectual disability, stem from the loss or partial loss of FMRP. This protein is encoded by the FMR1 gene, located on the X chromosome. Mutations in FMR1 lead to an excessive number of DNA triplet repeats, disrupting synapse formation and function. While there is no cure, therapies like physical therapy, speech therapy, and assistive technologies can help affected individuals.1
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