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Cell-Dependent Pathogenic Roles of Filamin B in Different Skeletal Malformations

Mutations of filamin B (FLNB) gene can lead to a spectrum of autosomal skeletal malformations including spondylocarpotarsal syndrome (SCT), Larsen syndrome (LRS), type I atelosteogenesis (AO1), type III atelosteogenesis (AO3), and boomerang dysplasia (BD). Among them, LRS is milder while BD causes a...

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Detalles Bibliográficos
Autores principales:	Wu, Huixiao, Wang, Yanzhou, Chen, Xinyu, Yao, Yangyang, Zhao, Wanyi, Fang, Li, Sun, Xiaoqing, Wang, Ning, Jiang, Jie, Gao, Ling, Zhao, Jiajun, Xu, Chao
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273461/ https://www.ncbi.nlm.nih.gov/pubmed/35832491 http://dx.doi.org/10.1155/2022/8956636

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