Publication | Closed Access
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome
42
Citations
41
References
2008
Year
Transcriptional RegulationGenetic DisorderNatural SciencesGeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationGene ExpressionMedicineSplicing VariantClinical Genetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1