Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function mutations and responds to pharmacological inhibition
Charles Bayard(Inserm), Guillaume Canaud(Hôpital Necker-Enfants Malades), Célia Chapelle(Hôpital Necker-Enfants Malades), Antoine Fraissenon(Université Claude Bernard Lyon 1), M.A.M. Taverne(Hôpital Necker-Enfants Malades), Baptiste Periou(Assistance Publique – Hôpitaux de Paris), François‐Jérôme Authier(Inserm), Thomas Viel(Inserm), Laurent Guibaud(Hospices Civils de Lyon), Ivan Nemazanyy(Centre National de la Recherche Scientifique), Lola Zerbib(Hôpital Necker-Enfants Malades), Sophia Ladraa(Inserm), Christine Broissand(Hôpital Necker-Enfants Malades), Arnaud Picard(Hôpital Necker-Enfants Malades), Jean–Paul Duong Van Huyen(Hôpital Necker-Enfants Malades), Gwennhaël Autret(Inserm), Nicolas Goudin(Délégation Paris 5), Christophe Legendre(Hôpital Necker-Enfants Malades), Michaël Dussiot(Laboratory of Excellence GR-Ex), B. Sergent(Hôpital Necker-Enfants Malades), Bertrand Tavitian(Inserm), Clément Hoguin(Inserm), Cyril Gitiaux(Hôpital Necker-Enfants Malades), E. Segna(Hôpital Necker-Enfants Malades), Quentin Hennocq(Hôpital Necker-Enfants Malades), Sophie Kaltenbach(Assistance Publique – Hôpitaux de Paris), Clarisse Delcros(Université Paris Cité), Roman Hossein Khonsari(Hôpital Necker-Enfants Malades), Sylvie Fraïtag(Délégation Paris 5), Vahid Asnafi(Hôpital Necker-Enfants Malades), Patrick Villarèse(Université Paris Cité)
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