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J.HRTHM.2008.01.020
J.HRTHM.2008.01.020
http://dx.doi.org/10.1016/J.HRTHM.2008.01.020
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.
P356
Q37193903-42509D04-332F-411B-8B39-3BB843FF3071
P356
J.HRTHM.2008.01.020
http://dx.doi.org/10.1016/J.HRTHM.2008.01.020