Genetics of mitochondrial diseases: Identifying mutations to help diagnosis
Mitochondrial diseases are amongst the most genetically and phenotypically diverse groups of inherited diseases. The vast phenotypic overlap with other disease entities together with the absence of reliable biomarkers act as driving forces for the integration of unbiased methodologies early in the d...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2020-06-01
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| Reeks: | EBioMedicine |
| Onderwerpen: | |
| Online toegang: | http://www.sciencedirect.com/science/article/pii/S2352396420301596 |
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