Literature DB >> 31593778

Decoding KCNH2 variants of unknown significance.

Carlos G Vanoye1, Alfred L George2.   

Abstract

Entities:  

Year:  2019        PMID： 31593778     DOI： 10.1016/j.hrthm.2019.10.009

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN： 1547-5271            Impact factor:   6.343


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  2 in total

1.  Serine mutation of a conserved threonine in the hERG K+ channel S6-pore region leads to loss-of-function through trafficking impairment.

Authors:  Ehab Al-Moubarak; Yihong Zhang; Christopher E Dempsey; Henggui Zhang; Stephen C Harmer; Jules C Hancox
Journal:  Biochem Biophys Res Commun       Date:  2020-04-19       Impact factor: 3.575

Review 2.  Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients.

Authors:  Makoto Ono; Don E Burgess; Elizabeth A Schroder; Claude S Elayi; Corey L Anderson; Craig T January; Bin Sun; Kalyan Immadisetty; Peter M Kekenes-Huskey; Brian P Delisle
Journal:  Biomolecules       Date:  2020-08-04
  2 in total

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