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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...
Tallennettuna:
| Julkaisussa: | Oncotarget |
|---|---|
| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Impact Journals LLC
2017
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| Aiheet: | |
| Linkit: | 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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