Author:
Peverelli Lorenzo,Catania Alessia,Marchet Silvia,Ciasca Paola,Cammarata Gabriella,Melzi Lisa,Bellino Antonella,Fancellu Roberto,Lamantea Eleonora,Capristo Mariantonietta,Caporali Leonardo,La Morgia Chiara,Carelli Valerio,Ghezzi Daniele,Bianchi Marzoli Stefania,Lamperti Costanza
Abstract
Leber's hereditary optic neuropathy (LHON) is due to missense point mutations affecting mitochondrial DNA (mtDNA); 90% of cases harbor the m.3460G>A, m.11778G>A, and m.14484T>C primary mutations. Here, we report and discuss five families with patients affected by symptomatic LHON, in which we found five novel mtDNA variants. Remarkably, these mtDNA variants are located in complex I genes, though without strong deleterious effect on respiration in cellular models: this finding is likely linked to the tissue specificity of LHON. This study observes that in the case of a strong clinical suspicion of LHON, it is recommended to analyze the whole mtDNA sequence, since new rare mtDNA pathogenic variants causing LHON are increasingly identified.
Subject
Neurology (clinical),Neurology
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献