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bibliographicCitation Carelli V, Sabatelli M, Carrozzo R, Rizza T, Schimpf S, Wissinger B, Zanna C, Rugolo M, La Morgia C, Caporali L, Carbonelli M, Barboni P, Tonon C, Lodi R, Bertini E. 'Behr syndrome' with OPA1 compound heterozygote mutations. Brain. 2015 Jan;138(Pt 1):e321. PMID: 25146916; PMCID: PMC4441076.
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