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Andrea Cavaliere

Unit of Medical Genetics and Neurogenetics

Fondazione IRCCS Istituto Neurologico Carlo Besta

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PUBLICATIONS

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

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Fondazione IRCCS Istituto Neurologico Carlo Besta

JOVE ARTICLES

An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model

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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Andrea Cavaliere

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Unit of Medical Genetics and Neurogenetics

Fondazione IRCCS Istituto Neurologico Carlo Besta

An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model

Unit of Medical Genetics and Neurogenetics