A rare optineurin mutation in an Indian family with coexistence of JOAG and PCG

PURPOSE: This study focused on the genetic screening of Myocilin (MYOC), Cytochrome P450 family 1 subfamily B member 1 (CYP1B1), Optineurin (OPTN), and SIX homeobox 6 (SIX6) genes in a family with coexistence of primary congenital glaucoma (PCG) and juvenile open-angle glaucoma (JOAG). METHODS: Sang...

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Detalles Bibliográficos
Autores principales: Yadav, Manoj, Yadav, Anshu, Bhardwaj, Aarti, Dhull, Chand Singh, Sachdeva, Sumit, Yadav, Ritu, Tanwar, Mukesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538844/
https://www.ncbi.nlm.nih.gov/pubmed/37530275
http://dx.doi.org/10.4103/IJO.IJO_3383_22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538844/
https://www.ncbi.nlm.nih.gov/pubmed/37530275
http://dx.doi.org/10.4103/IJO.IJO_3383_22

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