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Neuropsychiatric Disease and Treatment Volume 14, 2018 - Issue

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Letter

Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”

Tracey D GravesDepartment of Neurology, North West Anglia NHS Foundation Trust, Hinchingbrooke Hospital, Huntingdon, UK, [email protected]Correspondence[email protected]

Page 2329 | Published online: 11 Sep 2018

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Giulio Pulvirenti, Martina Caccamo, Manuela Lo Bianco, Marina Mazzurco, Elena R. Praticò, Alessandro Giallongo, Gloria Gangi, Antonio Zanghì & Raffaele Falsaperla. (2021) Calcium Channels Genes and Their Epilepsy Phenotypes. Journal of Pediatric Neurology 21:03, pages 224-234.
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Hannah C. Happ & Gemma L. Carvill. (2020) A 2020 View on the Genetics of Developmental and Epileptic Encephalopathies. Epilepsy Currents 20:2, pages 90-96.
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