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2 matching publication(s)
A potassium channel mutation in neonatal human epilepsy.
PMID 9430594 · Science (New York, N.Y.) · 1998
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A novel HRAS c.466C>T p.(Phe156Leu) variant in two patients with attenuated features of Costello syndrome.
PMID 35764878 · · 2022
L1
No computation