vwa1 Knockout in Zebrafish Causes Abnormal Craniofacial Chondrogenesis by Regulating FGF Pathway
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DOI: 10.3390/genes14040838
Abstract: Hemifacial microsomia (HFM), a rare disorder of first- and second-pharyngeal arch development, has been linked to a point mutation in VWA1 (von Willebrand factor A domain containing 1), encoding the protein WARP in a five-generation… read more here.
Keywords: vwa1 knockout; chondrogenesis; regulating fgf; fgf pathway ... See more keywords