P. Klemmer and Dr Ka Wan Li publish in J. of Biol. Chemistry
Fragile X syndrome, one of the most common inherited forms of X-linked mental retardation, is caused by a loss-of-function mutation of the Fmr1 gene on the X chromosome. The study, led by Patricia Klemmer and Dr Ka Wan Li in the neuroproteomics group at the VU University has just been published in the Journal of Biological Chemistry this month.
