R01 HL068854-06/HL/NHLBI NIH HHS/United States[Grants and Funding] - Search Results

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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 ZA, Momenah TS, Gong Q, Amin AS, Ghamdi SA, Carvalho JS, Homfray T, Mannens MM, Zhou Z, Wilde AA. Bhuiyan ZA, et al. Heart Rhythm. 2008 Apr;5(4):553-61. doi: 10.1016/j.hrthm.2008.01.020. Epub 2008 Jan 29. Heart Rhythm. 2008. PMID: 18362022 Free PMC article.

A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome.

Gong Q, Zhang L, Moss AJ, Vincent GM, Ackerman MJ, Robinson JC, Jones MA, Tester DJ, Zhou Z. Gong Q, et al. J Mol Cell Cardiol. 2008 Mar;44(3):502-9. doi: 10.1016/j.yjmcc.2008.01.002. Epub 2008 Jan 17. J Mol Cell Cardiol. 2008. PMID: 18272172 Free PMC article.

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