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Annals of Neurology
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April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel properties
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
American Journal of Human Genetics
|
April 2, 2021
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes
Carolina Courage, Karen L Oliver, Eon Joo Park, et al.
Nature Genetics
|
November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 33) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 33 results.
Annals of Neurology
|
April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel properties
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
American Journal of Human Genetics
|
April 2, 2021
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes
Carolina Courage, Karen L Oliver, Eon Joo Park, et al.
Nature Genetics
|
November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
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of 4