<i>vwa1</i> Knockout in Zebrafish Causes Abnormal Craniofacial Chondrogenesis by Regulating FGF Pathway

Hemifacial microsomia (HFM), a rare disorder of first- and second-pharyngeal arch development, has been linked to a point mutation in <i>VWA1</i> (von Willebrand factor A domain containing 1), encoding the protein WARP in a five-generation pedigree. However, how the <i>VWA1</i&g...

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Bibliographic Details
Main Authors: Xiaomin Niu, Fuyu Zhang, Lu Ping, Yibei Wang, Bo Zhang, Jian Wang, Xiaowei Chen
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/14/4/838