Three genetic mutations seen in individuals with KCNMA1-linked channelopathy successfully mirrored in mice - News-Medical.Net

Three genetic alterations associated with a rare seizure and a movement disorder primarily found in children were successfully mirrored in mice and their symptoms treated, in a new study from a University of Maryland School of Medicine researcher, Andrea Mere…

Three genetic alterations associated with a rare seizure and a movement disorder primarily found in children were successfully mirrored in mice and their symptoms treated, in a new study from a Unive… [+6680 chars]

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