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Article

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

31 Jan 2008

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Share to Cardiac Arrhythmias and Treatments
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 18362022
DOI: 10.1016/j.hrthm.2008.01.020

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