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pro vyhledávání: '"Chen L. Chew"'
Autor:
David J. Tester, Craig T. January, Chen L. Chew, Sadguna Y. Balijepalli, Kassandra E. Holzem, Sarah P. Concannon, Brian P. Delisle, Michael J. Ackerman, Ravi C. Balijepalli, Evi Lim
Background— Type 2 long QT syndrome involves mutations in the human ether a-go-go–related gene ( hERG or KCNH2 ). T421M, an S1 domain mutation in the Kv11.1 channel protein, was identified in a resuscitated patient. We assessed its biophysical, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad185b9da9386bdee4e9c1f926d1c1f2
https://europepmc.org/articles/PMC3530382/
https://europepmc.org/articles/PMC3530382/
