Even pore-localizing missense variants at highly conserved sites in KCNQ1-encoded Kv7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretation

Ashley Paquin, Dan Ye, David J. Tester, Jamie D. Kapplinger, Michael T. Zimmermann, Michael J. Ackerman

Research output: Contribution to journal › Article › peer-review

Fingerprint

Dive into the research topics of 'Even pore-localizing missense variants at highly conserved sites in KCNQ1-encoded Kv7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretation'. Together they form a unique fingerprint.