De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome

Jean Baptiste Rivière, Bregje W.M. Van Bon, Alexander Hoischen, Stanislav S. Kholmanskikh, Brian J. O'Roak, Christian Gilissen, Sabine Gijsen, Christopher T. Sullivan, Susan L. Christian, Omar A. Abdul-Rahman, Joan F. Atkin, Nicolas Chassaing, Valerie Drouin-Garraud, Andrew E. Fry, Jean Pierre Fryns, Karen W. Gripp, Marlies Kempers, Tjitske Kleefstra, Grazia M.S. Mancini, Małgorzata J.M. NowaczykConny M.A. Van Ravenswaaij-Arts, Tony Roscioli, Michael Marble, Jill A. Rosenfeld, Victoria M. Siu, Bert B.A. De Vries, Jay Shendure, Alain Verloes, Joris A. Veltman, Han G. Brunner, M. Elizabeth Ross, Daniela T. Pilz, William B. Dobyns

Research output: Contribution to journalArticlepeer-review

165 Scopus citations

Fingerprint Dive into the research topics of 'De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome'. Together they form a unique fingerprint.

Medicine & Life Sciences