FIGURE SUMMARY
- Title
-
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
- Authors
- Laquérriere, A., Maluenda, J., Camus, A., Fontenas, L., Dieterich, K., Nolent, F., Zhou, J., Monnier, N., Latour, P., Gentil, D., Héron, D., Desguerres, I., Landrieu, P., Beneteau, C., Delaporte, B., Bellesme, C., Baumann, C., Capri, Y., Goldenberg, A., Lyonnet, S., Bonneau, D., Estournet, B., Quijano-Roy, S., Francannet, C., Odent, S., Saint-Frison, M.H., Sigaudy, S., Figarella-Branger, D., Gelot, A., Mussini, J.M., Lacroix, C., Drouin-Garraud, V., Malinge, M.C., Attié-Bitach, T., Bessieres, B., Bonniere, M., Encha-Razavi, F., Beaufrère, A.M., Khung-Savatovsky, S., Perez, M.J., Vasiljevic, A., Mercier, S., Roume, J., Trestard, L., Saugier-Veber, P., Cordier, M.P., Layet, V., Legendre, M., Vigouroux-Castera, A., Lunardi, J., Bayes, M., Jouk, P.S., Rigonnot, L., Granier, M., Sternberg, D., Warszawski, J., Gut, I., Gonzales, M., Tawk, M., and Melki, J.
- Source
- Full text @ Hum. Mol. Genet.
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Acknowledgments