Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy-Reference-Cited by-同舟云学术

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

Published:2021-03-15 Issue:6 Volume:131 Page:
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

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

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

Link

https://www.jci.org/articles/view/138267/files/pdf