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FGF13 (fibroblast growth factor 13), belongs to the FGF family which are involved in cell growth, tissue repair, embryonic development and a number of other biological processes. FGF13 may also play a role in nervous system development/function. The location of this gene on chromosome X has been studied for links to Borjeson-Forssman-Lehmann syndrome (BFLS). FGF13 is known to have interactions with MAPK8IP2, SCN8A, CLEC3B, PRNP and EGFR.