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A recurrent de novo mutation in KCNC1 causes progressive ... | ResearchHub
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A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
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Authors
Mikko Muona
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Mikko Muona
•
Leanne Dibbens
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Anna-Elina Lehesjoki
Published
November 17, 2014
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Journal
Nature Genetics
Topics
Biology
Neuroscience
Rheumatology
Genetics
Molecular Biology
Show all topics
DOI
10.1038/ng.3144
