A Sprouty4 Mutation Identified in Kallmann Syndrome Increases the Inhibitory Potency of the Protein towards FGF and Connected Processes
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DOI: 10.3390/ijms22042145
Abstract: Kallmann syndrome is the result of innate genetic defects in the fibroblast growth factor (FGF) regulated signaling network causing diminished signal transduction. One of the rare mutations associated with the syndrome alters the Sprouty (Spry)4… read more here.
Keywords: protein; kallmann syndrome; spry4 protein; sprouty4 mutation ... See more keywords