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4 matching publication(s)
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
PMID 16964263 · Nature genetics · 2006
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A potassium channel mutation in neonatal human epilepsy.
PMID 9430594 · Science (New York, N.Y.) · 1998
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Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities.
PMID 35922433 · Nat Commun · 2022
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The focal adhesion protein β-parvin controls cardiomyocyte shape and sarcomere assembly in response to mechanical load.
PMID 35688156 · · 2022
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No computation