<i>PIK3CA</i> gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect
Quitterie Venot(Hôpital Necker-Enfants Malades), Guillaume Canaud(Hôpital Necker-Enfants Malades), Antoine Fraissenon(Université Claude Bernard Lyon 1), Charles Bayard(Inserm), G Morin(Inserm), Thomas Viel(Inserm), Laurent Guibaud(Hospices Civils de Lyon), Sanela Protic(Inserm), Sophia Ladraa(Inserm), Vahid Asnafi(Hôpital Necker-Enfants Malades), Gwennhaël Autret(Inserm), Nicolas Goudin(Délégation Paris 5), Alessandra Bolino(Vita-Salute San Raffaele University), Roberta Di Guardo(IRCCS Ospedale San Raffaele), Bertrand Tavitian(Inserm), Clément Hoguin(Inserm), Sato Magassa(Inserm), Sophie Kaltenbach(Assistance Publique – Hôpitaux de Paris), Franck Mayeux(Hôpital Necker-Enfants Malades), Marina Firpion(Inserm), Sylvie Fraïtag(Délégation Paris 5), Estelle Balducci(Inserm), Geneviève Gourdon(Inserm), Patrick Villarèse(Université Paris Cité)
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