Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction
- Hideki Itoh
- , Myriam Berthet
- , Véronique Fressart
- , Isabelle Denjoy
- , Svetlana Maugenre
- , Didier Klug
- , Yuka Mizusawa
- , Takeru Makiyama
- , Nynke Hofman
- , Birgit Stallmeyer
- , Sven Zumhagen
- , Wataru Shimizu
- , Arthur A. M. Wilde
- , Eric Schulze-Bahr
- , Minoru Horie
- , Sophie Tezenas du Montcel
- , Pascale Guicheney
Research output: Contribution to journal › Article › Academic › peer-review
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