A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects
Titel:
A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects
Auteur:
Beck, David B. Cho, Megan T. Millan, Francisca Yates, Carin Hannibal, Mark O’Connor, Bridget Shinawi, Marwan Connolly, Anne M. Waggoner, Darrel Halbach, Sara Angle, Brad Sanders, Victoria Shen, Yufeng Retterer, Kyle Begtrup, Amber Bai, Renkui Chung, Wendy K.