Publication | Open Access

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

Developmental AnomalyDevelopmental BiologyGenetic DisorderGeneticsGynecologyAneuploidyFunctional CharacterizationPrenatal DiagnosisFetal ComplicationMedicineNear AbsenceEmbryology