Publication
The clinical and molecular spectrum of
QRICH1
associated neurodevelopmental disorder
Smitha Kumble, Amanda M. Levy, Jaya Punetha, Hua Gao, Nicholas Ah Mew, Kwame Anyane‐Yeboa, Paul J. Benke, Sara M. Berger, Lise Bjerglund, Belinda Campos‐Xavier, Michael Ciliberto, Julie S. Cohen, Anne M. Comi, Cynthia Curry, Lena Damaj, Anne‐Sophie Denommé‐Pichon, Lisa Emrick, Laurence Faivre, Mary Beth Fasano, Alice Fiévet, Richard S. Finkel, Sixto García‐Miñaúr, Amanda Gerard, Paulino Gomez‐Puertas, Maria J. Guillen Sacoto, Trevor L. Hoffman, Lillian Howard, Alejandro D. Iglesias, Kosuke Izumi, Austin Larson, Anja Leiber, Reymundo Lozano, Iñigo Marcos‐Alcalde, Cassie S. Mintz, Sureni V. Mullegama, Rikke S. Møller, Sylvie Odent, Henry Oppermann, Elsebet Ostergaard, Marta Pacio‐Míguez, Maria Palomares‐Bralo, Sumit Parikh, Anna M. Paulson, Konrad Platzer, Jennifer E. Posey, Lorraine Potocki, Anya Revah‐Politi, Marlene Rio, Alyssa L. Ritter, Scott Robinson, Jill A. Rosenfeld, Fernando Santos‐Simarro, Sérgio B. Sousa, Mathys Wéber, Yili Xie, Wendy K. Chung, Natasha J. Brown, Zeynep Tümer
Human Mutation, December 2021, Hindawi Publishing Corporation
DOI: 10.1002/humu.24308