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Unit of Medical Genetics and Neurogenetics
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Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome.
Stem cell research Jan, 2021 | Pubmed ID: 33434818
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives.
Frontiers in neurology , 2021 | Pubmed ID: 34168607
Fondazione IRCCS Istituto Neurologico Carlo Besta
Andrea Cavaliere*,1,
Silvia Marchet*,1,
Ivano Di Meo1,
Valeria Tiranti1
1Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta
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