| Title | Authors | Year | Journal |
|---|---|---|---|
| Molecular and clinical genetics of mitochondrial diseases due to POLG mutations. | Truong CK | 2008 | Human mutation |
| Alpers syndrome with prominent white matter changes. | Truong CK | 2008 | Brain & development |
| Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI. | Truong CK | 2008 | Neuropediatrics |
Version:20250305
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