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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Detalhes bibliográficos
Publicado no:Front Cell Dev Biol
Main Authors: Wang, Yibei, Ping, Lu, Luan, Xiaodong, Chen, Yushan, Fan, Xinmiao, Li, Lianyan, Liu, Yaping, Wang, Pu, Zhang, Shuyang, Zhang, Bo, Chen, Xiaowei
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Cell and Developmental Biology
Acesso em linha: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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