A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia

BACKGROUND: Hemifacial microsomia (HFM) is a type of rare congenital syndrome caused by developmental disorders of the first and second pharyngeal arches that occurs in one out of 5,600 live births. There are significant gaps in our knowledge of the pathogenic genes underlying this syndrome. METHODS...

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Bibliografiska uppgifter
I publikationen:Front Cell Dev Biol
Huvudupphovsmän: Wang, Yibei, Ping, Lu, Luan, Xiaodong, Chen, Yushan, Fan, Xinmiao, Li, Lianyan, Liu, Yaping, Wang, Pu, Zhang, Shuyang, Zhang, Bo, Chen, Xiaowei
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2020
Ämnen:
Cell and Developmental Biology
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7509151/
https://ncbi.nlm.nih.gov/pubmed/33015062
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.571004
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