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Focal segmental glomerulosclerosis associated with mitochondrial disease
Primary mitochondrial diseases (MD) are complex, heterogeneous inherited diseases caused by mutations in either the mitochondrial or nuclear DNA. Glomerular diseases in MD have been reported with tRNA mutation m.3243A>G causing a syndrome of mitochondrial encephalomyopathy, lactic acidosis and st...
Tallennettuna:
| Julkaisussa: | Clin Nephrol Case Stud |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Dustri-Verlag Dr. Karl Feistle
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438005/ https://ncbi.nlm.nih.gov/pubmed/29043143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/CNCS109083 |
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