Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

Zahurul A. Bhuiyan, Tarek S. Momenah, Qiuming Gong, Ahmad S. Amin, Saleh Al Ghamdi, Julene S. Carvalho, Tessa Homfray, Marcel M.A.M. Mannens, Zhengfeng Zhou, Arthur A.M. Wilde

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Medicine & Life Sciences