Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategies
改善法国转甲状腺素蛋白淀粉样变性基因检测途径:挑战与策略
期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-024-03370-z
Hebrard, Bérénice; Babonneau, Marie-Lise; Charron, Philippe; Consolino, Emilie; Dauriat, Benjamin; Dupin-Deguine, Delphine; Fargeaud, Dominique; Farrugia, Agnès; Giguet-Valard, Anna-Gaëlle; Guijarro, Damien; Inamo, Jocelyn; Jeanneteau, Julien; Mazzella, Jean-Michaël; Michon, Claire-Cécile; Millat, Gilles; Mouquet, Frédéric; Oghina, Silvia; Pereon, Yann; Poinsignon, Vianney; Pompougnac, Julie; Proukhnitzky, Julie; Schaefer, Elise; Sturtz, Franck; Trosdorf, Mathilde; Auguste, Anne; Canali, Giorgia; Combes, Alexandre; Funalot, Benoît; Damy, Thibaud