Carrara F
Publications:
| Title | Authors | Year | Journal |
|---|---|---|---|
| Clinical and molecular features of mitochondrial DNA depletion syndromes. | Carrara F | 2009 | Journal of inherited metabolic disease |
| Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonism. | Carrara F | 2008 | Neuromuscular disorders : NMD |
| Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA. | Carrara F | 2005 | Brain : a journal of neurology |
| Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO). | Carrara F | 2003 | Neurology |
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