CHST6 mutation screening and endoplasmatic reticulum stress in macular corneal dystrophy

Macular corneal dystrophy (MCD) is an autosomal recessive disorder mainly caused by gene mutations of carbohydrate sulfotransferase (CHST6) leading to bilateral visual impairment. Because the mechanism underlying this degeneration remains poorly understood, we investigated molecular alterations and...

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Detalles Bibliográficos
Autores principales: Wang, Liyuan, Tang, Xianling, Lv, Xiaolin, Sun, Encheng, Wu, Donglai, Wang, Changlin, Liu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707101/
https://www.ncbi.nlm.nih.gov/pubmed/29221207
http://dx.doi.org/10.18632/oncotarget.22028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707101/
https://www.ncbi.nlm.nih.gov/pubmed/29221207
http://dx.doi.org/10.18632/oncotarget.22028

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