A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family

PURPOSE: Peters anomaly (PA) is a heterogeneous developmental disorder characterized by central corneal opacity and iridocorneal or corneolenticular adhesions. Although many causative genes have been identified, most screened patients do not have mutations in the known genes. We aimed to identify th...

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Detalles Bibliográficos
Autores principales: Darbari, Ensieh, Zare-Abdollahi, Davood, Alavi, Afagh, Rezaei Kanavi, Mozhgan, Feizi, Sepehr, Hosseini, Seyed Bagher, Baradaran-Rafii, Alireza, Ahmadieh, Hamid, Issazadeh-Navikas, Shohreh, Elahi, Elahe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700884/
https://www.ncbi.nlm.nih.gov/pubmed/33273802

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700884/
https://www.ncbi.nlm.nih.gov/pubmed/33273802

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