טוען...
Altered Mitochondrial Function in Type 2 Granular Corneal Dystrophy
Type 2 granular corneal dystrophy (GCD2) is caused by point mutation R124H in the transforming growth factor-β–induced gene (TGFBI) and is characterized by age-dependent progression of corneal deposits. Mitochondrial features in heterozygous GCD2 and normal corneal tissues was evaluated using electr...
שמור ב:
| Main Authors: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Investigative Pathology
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3157179/ https://ncbi.nlm.nih.gov/pubmed/21699880 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2011.04.005 |
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