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Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant
Beryll Blickhaeuser, Sarah L. Stenton, Christiane M. Neuhofer (Co-author), Elisa Floride (Co-author), Victoria Nesbitt, Carl Fratter, Johannes Koch (Co-author), Birgit Kauffmann, Claudia Catarino, Lea Dewi Schlieben, Robert Kopajtich, Valerio Carelli, Alfredo A. Sadun, Robert McFarland, Fang Fang, Chiara La Morgia, Stephanie Paquay, Marie Cecile Nassogne, Daniele Ghezzi, Costanza Lamperti
- University of Technology Munich
- MD, MPH Mandy Brown Belfort, Harvard University
- Technical University of Munich
- Amalia Childrens Hosp
- Klinikum Bremen-Mitte
- Technical University of Munich Weihenstephan-Triesdorf University of Applied Sciences
- Doheny Eye Institute
- Capital Medical University
- Universite Catholique Louvain
- Fondazione IRCCS Istituto Nazionale Tumori Milan
- University of Milan-Bicocca
- Amalia Children's Hospital
- Department of Neuroradiology; University of Oxford; Prof. J.V. Byrne
Research output: Contribution to journal › Original Article (Journal) › peer-review
2
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(Web of Science)