Heterogeneity of Axenfeld–Rieger Syndrome: Molecular and Clinical Findings in Chinese Patients

Axenfeld–Rieger Syndrome (ARS) is a rare disease with a wide spectrum of ocular and systemic manifestations. The genetic spectrum of Chinese patients with ARS and genotype-phenotype correlations have yet to be described. To explore the molecular and clinical features in Chinese patients, fifty-five...

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Detalles Bibliográficos
Autores principales: Zhang, Youjia, Chen, Xueli, Wang, Li, Sun, Xinghuai, Chen, Yuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564140/
https://www.ncbi.nlm.nih.gov/pubmed/34745210
http://dx.doi.org/10.3389/fgene.2021.732170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564140/
https://www.ncbi.nlm.nih.gov/pubmed/34745210
http://dx.doi.org/10.3389/fgene.2021.732170

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