Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
Titel:
Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
Auteur:
Kopajtich, Robert Nicholls, Thomas J. Rorbach, Joanna Metodiev, Metodi D. Freisinger, Peter Mandel, Hanna Vanlander, Arnaud Ghezzi, Daniele Carrozzo, Rosalba Taylor, Robert W. Marquard, Klaus Murayama, Kei Wieland, Thomas Schwarzmayr, Thomas Mayr, Johannes A. Pearce, Sarah F. Powell, Christopher A. Saada, Ann Ohtake, Akira Invernizzi, Federica Lamantea, Eleonora Sommerville, Ewen W. Pyle, Angela Chinnery, Patrick F. Crushell, Ellen Okazaki, Yasushi Kohda, Masakazu Kishita, Yoshihito Tokuzawa, Yoshimi Assouline, Zahra Rio, Marlène Feillet, François Mousson de Camaret, Bénédict Chretien, Dominique Munnich, Arnold Menten, Björn Sante, Tom Smet, Joél Régal, Luc Lorber, Abraham Khoury, Asaad Zeviani, Massimo Strom, Tim M. Meitinger, Thomas Bertini, Enrico S. Van Coster, Rudy Klopstock, Thomas Rötig, Agnès Haack, Tobias B. Minczuk, Michal Prokisch, Holger