A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

Abstract Mutations in the Forkhead Box C1 (FOXC1) are known to cause autosomal dominant hereditary Axenfeld-Rieger syndrome, which is a genetic disorder characterized by ocular and systemic features including glaucoma, variable dental defects, craniofacial dysmorphism and hearing loss. Due to late-o...

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Autores principales: Rui Wang, Wei-Qian Wang, Xiao-Qin Li, Juan Zhao, Kun Yang, Yong Feng, Meng-Meng Guo, Min Liu, Xing Liu, Xi Wang, Yong-Yi Yuan, Xue Gao, Jin-Cao Xu
Formato: article
Lenguaje:EN
Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/01e95e3556b74eb9b9985d9b000e849b
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