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Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation
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.Volume:
5
Year:
2008
Language:
english
DOI:
10.1016/j.hrthm.2008.01.020
File:
PDF, 3.20 MB
english, 2008