GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates
Titel:
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates
Auteur:
Ouyang, Qing Kavanaugh, Brian C. Joesch-Cohen, Lena Dubois, Bethany Wu, Qing Schmidt, Michael Baytas, Ozan Pastore, Stephen F. Harripaul, Ricardo Mishra, Sasmita Hussain, Abrar Kim, Katherine H. Holler-Managan, Yolanda F. Ayub, Muhammad Mir, Asif Vincent, John B. Liu, Judy S. Morrow, Eric M.