Activating mutations in FGFR3 tyrosine kinase cause several forms of human skeletal dysplasia. Although the mechanisms of FGFR3 action in cartilage are not completely understood. it is believed that the STAT1 transcription factor plays a central role in pathogenic FGFR3 signaling. Here. https://fitnessgravesyardes.shop/product-category/tv-bracket/