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UnknownPost-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases.
Not available
S-EPMC7782403 | biostudies-literature
UnknownVariant interpretation in molecular autopsy: a useful dilemma.
Not available
S-EPMC8847204 | biostudies-literature
UnknownCharacterization of an N-terminal Nav1.5 channel variant - a potential risk factor for arrhythmias and sudden death?
Not available
S-EPMC7678220 | biostudies-literature
UnknownMolecular phylogeny and evolution of the cone snails (Gastropoda, Conoidea).
Not available
S-EPMC5556946 | biostudies-literature
Unknown"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".
Not available
S-EPMC11282671 | biostudies-literature
UnknownCorrection: "Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".
Not available
S-EPMC11529073 | biostudies-literature
UnknowniNOS expressing macrophages co-localize with nitrotyrosine staining after myocardial infarction in humans.
Not available
S-EPMC10098457 | biostudies-literature
UnknownChanges in gene expression patterns in postmortem human myocardial infarction.
Not available
S-EPMC7417407 | biostudies-literature
UnknownThe mutation L69P in the PAS domain of the hERG potassium channel results in LQTS by trafficking deficiency.
Not available
S-EPMC7188350 | biostudies-literature
UnknownPotassium channel TASK-5 forms functional heterodimers with TASK-1 and TASK-3 to break its silence.
Not available
S-EPMC11364637 | biostudies-literature
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