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by Heard, Jean-Michel and Bellettato, Cinzia and Van Lingen, Corine and Scarpa, Maurizio and Debray, François-Guillaume and Nassogne, Marie-Cécile and Van Coster, Rudy and De Meirleir, Linda and Eyskens, François and Morava, Eva and Baric, Ivo and Kozich, Viktor and Lund, Allan Meldgaard and Germain, Dominique and Belmatoug, Nadia and Guffon, Nathalie and Labrune, Philippe and Gouya, Laurent and De Lonlay, Pascale and Schiff, Manuel and Dobbelaere, Dries and Chabrol, Brigitte and Das, Anihb Martin and Spiekerkoetter, Ute and Rutsch, Frank and Ploeckinger, Ursula and Mohnike, Klaus and Hahn, Andreas and Kölker, Stefan and Ullrich, Kurt and Balogh, István and Bembi, Bruno and Donati, Maria Alice and Gasperini, Serena and Parenti, Giancarlo and Salviati, Alessandro and Vici, Carlo-Dionisi and Di Rocco, Maja and Cefalo, Graziella and Burlina, Alberto and Ceccarini, Giovanni and Federico, Antonio and Van Der Ploeg, Ans and Rubio-Gozalbo, Maria-Estela and Van Spronsen, Francian and Visser, Gepke and Bosch, Annet and Tangeraas, Trine and Sanderberg, Sverre and Kieć-Wilk, Beata and Gaspar, Ana-Maria Simões Mendes and Martins, Esmeralda and Silva, Esmeralda-Maria Ferreira Rodrigues and De Abreu Freire Diogo Matos, Luísa-Maria and Azevedo, Olga and Tansek, Mojca-Zerjav and Couce-Pico, Maria-Luz and Cazorla, Angeles Garcia and Azuara, Luis Aldámiz-Echevarría and Del Toro-Riera, Mireia and Lajic, Svetlana and Darin, Niklas and Deegan, Patrick and Vijaym, Suresh and Chronopoulou, Efstathia and Jones, Simon and Chakrapani, Anupanm and Hiwot, Tarekegn and MetabERN collaboration group and the MetabERN collaboration group
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 05/2019, Volume 14, Issue 1, pp. 119 - 9
Journal Article
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