Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy

Author:

Stenton Sarah L.ORCID,Sheremet Natalia L.ORCID,Catarino Claudia B.ORCID,Andreeva Natalia A.,Assouline Zahra,Barboni Piero,Barel Ortal,Berutti RiccardoORCID,Bychkov Igor,Caporali LeonardoORCID,Capristo Mariantonietta,Carbonelli Michele,Cascavilla Maria L.,Charbel Issa PeterORCID,Freisinger Peter,Gerber Sylvie,Ghezzi DanieleORCID,Graf ElisabethORCID,Heidler Juliana,Hempel Maja,Heon EliseORCID,Itkis Yulya S.,Javasky Elisheva,Kaplan Josseline,Kopajtich Robert,Kornblum Cornelia,Kovacs-Nagy Reka,Krylova Tatiana D.,Kunz Wolfram S.,La Morgia ChiaraORCID,Lamperti Costanza,Ludwig Christina,Malacarne Pedro F.,Maresca Alessandra,Mayr Johannes A.ORCID,Meisterknecht Jana,Nevinitsyna Tatiana A.,Palombo FlaviaORCID,Pode-Shakked Ben,Shmelkova Maria S.ORCID,Strom Tim M.,Tagliavini Francesca,Tzadok Michal,van der Ven Amelie T.,Vignal-Clermont CatherineORCID,Wagner MatiasORCID,Zakharova Ekaterina Y.,Zhorzholadze Nino V.,Rozet Jean-Michel,Carelli ValerioORCID,Tsygankova Polina G.,Klopstock ThomasORCID,Wittig Ilka,Prokisch HolgerORCID

Funder

German Federal Ministry of Education and Research (BMBF, Bonn, Germany) grant to the German Network for Mitochondrial Disorders

German BMBF and Horizon2020 through the E-Rare project GENOMIT

Deutsche Forschungsgemeinschaft

Italian Ministry of Health

Cardio Pulmonary Institute (CPI) of the DFG

Publisher

American Society for Clinical Investigation

Subject

General Medicine

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