Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategies.

Autor: Hebrard, Bérénice1,2,3,4 (AUTHOR), Babonneau, Marie-Lise3 (AUTHOR), Charron, Philippe3,5 (AUTHOR), Consolino, Emilie3,4,6 (AUTHOR), Dauriat, Benjamin3,7 (AUTHOR), Dupin-Deguine, Delphine3,8 (AUTHOR), Fargeaud, Dominique2,3,9 (AUTHOR), Farrugia, Agnès10 (AUTHOR), Giguet-Valard, Anna-Gaëlle11,12 (AUTHOR), Guijarro, Damien2,13 (AUTHOR), Inamo, Jocelyn2,11,12 (AUTHOR), Jeanneteau, Julien2,14 (AUTHOR), Mazzella, Jean-Michaël3,4,6 (AUTHOR), Michon, Claire-Cécile3 (AUTHOR), Millat, Gilles3,15 (AUTHOR), Mouquet, Frédéric16 (AUTHOR), Oghina, Silvia2,3,17 (AUTHOR), Pereon, Yann12,18 (AUTHOR), Poinsignon, Vianney12,19 (AUTHOR), Pompougnac, Julie2,3,17 (AUTHOR)
Zdroj: Orphanet Journal of Rare Diseases. 10/29/2024, Vol. 19, p1-7. 7p.
Databáze: Academic Search Ultimate
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