Modeling MELAS-associated cardiac defects using patient-specific iPSC-derived cardiomyocytes and cardiac organoids
Mitochondrial diseases are a diverse family of maternally-inherited disorders that often result from mitochondrial DNA (mtDNA) mutations. These disorders are mostly heterogeneous and manifest as a broad spectrum of clinical phenotypes among patients. In this study, we will be utilising patient-speci...
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| Format: | Final Year Project (FYP) |
| Language: | English |
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2018
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| Online Access: | http://hdl.handle.net/10356/74163 |