Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses | Journal of Medical Genetics

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Neurogenetics

Original article

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

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Cite this article as:: Addis L, Sproviero W, Thomas SV, et al

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

Journal of Medical Genetics 2018;55:607-616.