Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation
Titel:
Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation
Auteur:
Bhuiyan, Zahurul A. Momenah, Tarek S. Gong, Qiuming Amin, Ahmad S. Ghamdi, Saleh Al Carvalho, Julene S. Homfray, Tessa Mannens, Marcel M.A.M. Zhou, Zhengfeng Wilde, Arthur A.M.