Diencephalic Size Is Restricted by a Novel Interplay Between GCN5 Acetyltransferase Activity and Retinoic Acid Signaling
Jonathan J. Wilde(McGovern Institute for Brain Research), Lee Niswander(University of Colorado Boulder)
Cited by 24
Related Papers
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
|Human Molecular Genetics|2014|151