| Title | Authors | Year | Journal |
|---|---|---|---|
| Digenic mutations in severe myoclonic epilepsy of infancy. | Hinttala R | 2009 | Epilepsy research |
| Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus. | Hinttala R | 2008 | Epilepsia |
| Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene. | Hinttala R | 2008 | Parkinsonism & related disorders |
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