Valerio Carelli
IRCCS Istituto Delle Scienze Neurologiche di Bologna
217 papers found
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Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus
Download from www.researchgate.netOPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.
Download from academic.oup.comEvidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy
Download from www.researchgate.netBiochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993
Download from www.researchgate.netMitochondrial Optic Neuropathies: How Two Genomes may Kill the Same Cell Type?
Download from portlandpress.comLeber's Hereditary Optic Neuropathy with Childhood Onset
Download from iovs.arvojournals.orgThe role of mitochondria in health, ageing, and diseases affecting vision
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