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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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| 發表在: | Oncotarget |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Impact Journals LLC
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5707101/ https://ncbi.nlm.nih.gov/pubmed/29221207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.22028 |
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