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

@article{Bhuiyan2008RecurrentIF,
  title={Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.},
  author={Zahurul A Bhuiyan and Tarek Sulaiman Momenah and Qiuming Gong and Ahmad Shoaib Amin and Saleh Al Ghamdi and Julene S Carvalho and Tessa Homfray and Marcel M. A. M. Mannens and Zhengfeng Zhou and Arthur A. M. Wilde},
  journal={Heart rhythm},
  year={2008},
  volume={5 4},
  pages={553-61}
}
BACKGROUND Inherited arrhythmias may underlie intrauterine and neonatal arrhythmias. Resolving the molecular genetic nature of these rare cases provides significant insight into the role of the affected proteins in arrhythmogenesis and (extra-) cardiac development. OBJECTIVE The purpose of this study was to perform clinical, molecular, and functional studies of a consanguineous Arabian family with repeated early miscarriages and two intrauterine fetal losses in the early part of the third… CONTINUE READING
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