vwa1 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 VWA1 (von Willebrand factor A domain containing 1), encoding the protein WARP in a five-generation pedigree. However, how the VWA1 mutation relates to the pathogenesi...

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Detalles Bibliográficos
Autores principales: Niu, Xiaomin, Zhang, Fuyu, Ping, Lu, Wang, Yibei, Zhang, Bo, Wang, Jian, Chen, Xiaowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137681/
https://www.ncbi.nlm.nih.gov/pubmed/37107596
http://dx.doi.org/10.3390/genes14040838

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137681/
https://www.ncbi.nlm.nih.gov/pubmed/37107596
http://dx.doi.org/10.3390/genes14040838

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