Mice harboring the FXN I151F pathological point mutation present decreased frataxin levels, a Friedreich ataxia-like phenotype, and mitochondrial alterations

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2022
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Medina Carbonero, MartaMedina Carbonero, Marta - ORCID ID
Sanz Alcázar, Arabela
Britti, ElenaBritti, Elena - ORCID ID
Delaspre, FabienDelaspre, Fabien - ORCID ID
Cabiscol Català, ElisaCabiscol Català, Elisa - ORCID ID
Ros Salvador, JoaquimRos Salvador, Joaquim - ORCID ID
Tamarit Sumalla, JordiTamarit Sumalla, Jordi - ORCID ID
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