Cargando…
Novel Compound Heterozygous Variations in MPDZ Gene Caused Isolated Bilateral Macular Coloboma in a Chinese Family
Macular coloboma (MC) is a rare congenital retinochoroidal defect characterized by lesions of different sizes in the macular region. The pathological mechanism underlying congenital MC is unknown. Novel compound heterozygous variations, c.4301delA (p.Asp1434fs*3) and c.5255C>G (p.Ser1752Ter), in...
Autores principales: | Zhang, Shuang, Zhang, Fangxia, Wang, Juan, Yang, Shangying, Ren, Yinghua, Rui, Xue, Xia, Xiaobo, Sheng, Xunlun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688216/ https://www.ncbi.nlm.nih.gov/pubmed/36429029 http://dx.doi.org/10.3390/cells11223602 |
Ejemplares similares
-
Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma
por: Li, Tao, et al.
Publicado: (2017) -
Evaluating the association between MPDZ-NF1B rs1324183 and keratoconus in an independent northwestern Chinese population
por: Yuan, Shiqin, et al.
Publicado: (2022) -
Macular coloboma
por: Varghese, Mary, et al.
Publicado: (2016) -
Bilateral congenital macular coloboma and cataract: A case report
por: Zhang, Canwei, et al.
Publicado: (2019) -
Achondroplasia and Macular Coloboma
por: Ahoor, M. H., et al.
Publicado: (2015)