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You searched for: Author/Creator Tester, David J

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1. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry. (6th June 2019)

2. Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study. Issue 10129 (14th April 2018)

3. KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1. Issue 6 (6th March 2017)

5. SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups. (27th July 2018)

6. Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site. Issue 11 (13th August 2019)