De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome
Titel:
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome
Auteur:
Burrage, Lindsay C. Charng, Wu-Lin Eldomery, Mohammad K. Willer, Jason R. Davis, Erica E. Lugtenberg, Dorien Zhu, Wenmiao Leduc, Magalie S. Akdemir, Zeynep C. Azamian, Mahshid Zapata, Gladys Hernandez, Patricia P. Schoots, Jeroen de Munnik, Sonja A. Roepman, Ronald Pearring, Jillian N. Jhangiani, Shalini Katsanis, Nicholas Vissers, Lisenka E.L.M. Brunner, Han G. Beaudet, Arthur L. Rosenfeld, Jill A. Muzny, Donna M. Gibbs, Richard A. Eng, Christine M. Xia, Fan Lalani, Seema R. Lupski, James R. Bongers, Ernie M.H.F. Yang, Yaping