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Publications by Emmy Räkers
Phenotypic Characterization of an Older Adult Male With Late-Onset Epilepsy and a Novel Mutation in ASXL3 Shows Overlap With the Associated Bainbridge-Ropers Syndrome
Neuropsychiatric Disease and Treatment
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Phenotypic Diversity of Myoclonus Epilepsy Associated With Ragged-Red Fibers With an 8344A>G mtDNA Mutation
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UBR5Gene Mutation Is Associated With Familial Adult Myoclonic Epilepsy in a Japanese Family
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Clinical and Electrophysiological Characterization of a Novel Mutation (F193L) in the KCNQ1 Gene Associated With Long QT Syndrome
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