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Fressart, Véronique

https://orcid.org/0000-0003-4749-1428

A5008670843 | I4210097159

Assistance Publique – Hôpitaux de Paris

Citations 2

SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

European Heart Journal | July 3, 2018 | Volume: 39 | Issue: 31 | Pages: 2879-2887

10.1093/eurheartj/ehy412 | PMID 30059973

High-Risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K+ Permeation

Biochemistry | October 23, 2012 | Volume: 51 | Issue: 45 | Pages: 9076-9085

10.1021/bi3009449 | PMID 23092362