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A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy.
Not available
S-EPMC2707221
|
biostudies-literature
Cite
Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for
KCND3
-Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes.
Not available
S-EPMC9588492
|
biostudies-literature
Cite
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.
Not available
S-EPMC5035208
|
biostudies-literature
Cite
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.
Not available
S-EPMC5834028
|
biostudies-literature
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Localized Structural Alterations Underlying a Subset of Unexplained Sudden Cardiac Death.
Not available
S-EPMC7661047
|
biostudies-literature
Cite
Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry.
Not available
S-EPMC7439932
|
biostudies-literature
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Functional consequences of allotypic polymorphisms in human immunoglobulin G subclasses.
Not available
S-EPMC9845132
|
biostudies-literature
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Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.
Not available
S-EPMC2810855
|
biostudies-literature
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SCN5A
Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in
SCN5A
Families.
Not available
S-EPMC7748043
|
biostudies-literature
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Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Not available
S-EPMC6394853
|
biostudies-literature
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