Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
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author: Sylvie Odent, Valérie Layet, Marie-Pierre Cordier, Alice Goldenberg, Tania Attié-Bitach, Stanislas Lyonnet, Dominique Figarella-Branger, Laura Fontenas, Flora Nolent, Marcel Tawk, Dominique Bonneau, Delphine Héron, Clarisse Baumann, Yline Capri, Judith Melki, Christine Francannet
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