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(28)
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(6)
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(41)
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(38)
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(38)
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Department of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Korea
(1)
Department of Physiology and Cellular Biophysics, Columbia University Irving Medical Center, New York, NY
(1)
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(1)
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Tags
xref:PubMed:31857479
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xref:PubMed:41986745
(1)
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CACNA1H mutation
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Dimethylglycine dehydrogenase deficiency
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Whole genome sequencing in paediatric channelopathy and cardiomyopathy.
Not available
S-EPMC10997036
|
biostudies-literature
Cite
Combinatorial chloride and calcium channelopathy in myotonic dystrophy.
Not available
S-EPMC10312834
|
biostudies-literature
Cite
Whole Genome Sequencing in Paediatric Channelopathy and Cardiomyopathy
PRJNA1086226
|
ENA
Cite
KCNMA1
-linked channelopathy.
Not available
S-EPMC6785733
|
biostudies-literature
Cite
Channelopathy pathogenesis in a human neural cell model of Angelman Syndrome
Channelopathy pathogenesis in a human neural cell model of Angelman Syndrome
PRJNA492237
|
ENA
Cite
Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?
Not available
S-EPMC9602309
|
biostudies-literature
Cite
Verapamil mitigates chloride and calcium bi-channelopathy in a myotonic dystrophy mouse model.
Not available
S-EPMC10760957
|
biostudies-literature
Cite
Channelopathy Genes in Pulmonary Arterial Hypertension.
Not available
S-EPMC8961593
|
biostudies-literature
Cite
Mechanistic ion channel interactions in red cells of patients with Gardos channelopathy.
Not available
S-EPMC8525243
|
biostudies-literature
Cite
Anxiety and depression in inherited channelopathy patients with implantable cardioverter-defibrillators.
Not available
S-EPMC8369306
|
biostudies-literature
Cite
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