Novel mutations of the PAX6, FOXC1, and PITX2 genes cause abnormal development of the iris in Vietnamese individuals

PURPOSE: Congenital iris abnormality is a feature of several genetic conditions, such as aniridia syndrome and anterior segment degeneration (ASD) disorders. Aniridia syndrome is caused by mutations in the PAX6 gene or its regulatory elements in the locus 11p13 or deletions of contiguous genes, whil...

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Detalles Bibliográficos
Autores principales: Nguyen, Ha Hai, Pham, Chau Minh, Nguyen, Hoa Thi Thanh, Vu, Nhung Phuong, Duong, Trang Thu, Nguyen, Ton Dang, Nguyen, Bac Duy, Nguyen, Hiep Van, Nong, Hai Van
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416135/
https://www.ncbi.nlm.nih.gov/pubmed/34566401

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416135/
https://www.ncbi.nlm.nih.gov/pubmed/34566401

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