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Study supported by: Italian Ministry of Health (Ricerca Finalizzata Grant: RF-2018-12366703) and MITOCON (Italian association for the study and treatment of Mithocondrial Diseases (Grant no. 2018-01)
genetic analysis related to article "Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber’s Hereditary Optic Neuropathy (LHON)"
Human iPSC cells, Leber's Hereditary opticNeuropathy, mutation
Human iPSC cells, Leber's Hereditary opticNeuropathy, mutation
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
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