Concepedia

Publication | Open Access

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

DOIFull Paper Access

311

Citations

66

References

2014

Year

Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens, Karen Oliver, Snezana Maljevic, Marta A. Bayly, Tarja Joensuu, Laura Canafoglia, Silvana Franceschetti, Roberto Michelucci,
Nature Genetics

References

YearCitations

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