טוען...
De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans
Defects in the mitochondrial genome (mitochondrial DNA (mtDNA)) are associated with both congenital and acquired disorders in humans. Nuclear-encoded DNA polymerase subunit gamma (POLG) plays an important role in mtDNA replication, and proofreading and mutations in POLG have been linked with increas...
שמור ב:
| הוצא לאור ב: | Genes (Basel) |
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| Main Authors: | , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
MDPI
2021
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7922481/ https://ncbi.nlm.nih.gov/pubmed/33671400 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12020284 |
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