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Bénédict Mousson de Camaret
Publications - 1
Citations - 120
Bénédict Mousson de Camaret is an academic researcher. The author has contributed to research in topics: Human mitochondrial genetics & Mitochondrial DNA. The author has an hindex of 1, co-authored 1 publications receiving 99 citations.
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Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
Robert Kopajtich,Thomas J. Nicholls,Joanna Rorbach,Metodi D. Metodiev,Peter Freisinger,Hanna Mandel,Arnaud Vanlander,Daniele Ghezzi,Rosalba Carrozzo,Robert W. Taylor,Klaus Marquard,Kei Murayama,Thomas Wieland,Thomas Schwarzmayr,Johannes A. Mayr,Sarah F. Pearce,Christopher A. Powell,Ann Saada,Akira Ohtake,Federica Invernizzi,Eleonora Lamantea,Ewen W. Sommerville,Angela Pyle,Patrick F. Chinnery,Ellen Crushell,Yasushi Okazaki,Masakazu Kohda,Yoshihito Kishita,Yoshimi Tokuzawa,Zahra Assouline,Marlène Rio,François Feillet,Bénédict Mousson de Camaret,Dominique Chretien,Arnold Munnich,Arnold Munnich,Björn Menten,Tom Sante,Joél Smet,Luc Régal,Abraham Lorber,Asaad Khoury,Massimo Zeviani,Tim M. Strom,Thomas Meitinger,Enrico Bertini,Rudy Van Coster,Thomas Klopstock,Agnès Rötig,Tobias B. Haack,Michal Minczuk,Holger Prokisch +51 more
TL;DR: The study of a mitochondrial translation disorder points toward the importance of posttranscriptional modification of mitochondrial tRNAs for proper mitochondrial function.