Researchers at the Department of Molecular Genetics, University of Antwerp, and other centers in Belgium, The Netherlands, and Melbourne, Australia, analyzed the clinical phenotypes associated with STXBPl mutations in a cohort of 106 patients with unexplained early-onset epileptic encephalopathies.

Millichap, J.G. (0AD) ‘Early-Onset Epileptic Encephalopathies with STXBPl Mutations’, Pediatric Neurology Briefs, {volume}({issue}), p. {page}. Available at: https://doi.org/10.15844/pedneurbriefs-24-12-1.

Millichap, J G. “Early-Onset Epileptic Encephalopathies with STXBPl Mutations”. Pediatric Neurology Briefs, vol. {volume}, no. {issue}, 0AD, p. {page}, doi:10.15844/pedneurbriefs-24-12-1.

Millichap, J. G. (0AD). Early-Onset Epileptic Encephalopathies with STXBPl Mutations. Pediatric Neurology Briefs, {volume}({issue}), {page}. https://doi.org/10.15844/pedneurbriefs-24-12-1

Millichap, J Gordon. 0AD. “Early-onset Epileptic Encephalopathies with Stxbpl Mutations”. Pediatric Neurology Briefs {volume} ({issue}): {page}. https://doi.org/10.15844/pedneurbriefs-24-12-1.

1. Millichap JG. Early-Onset Epileptic Encephalopathies with STXBPl Mutations. Pediatric Neurology Briefs. 0AD;{volume}({issue}):{page}. DOI: https://doi.org/10.15844/pedneurbriefs-24-12-1

1. Millichap JG. Early-Onset Epileptic Encephalopathies with STXBPl Mutations. Pediatric Neurology Briefs. 0AD;{volume}({issue}):{page}. doi:10.15844/pedneurbriefs-24-12-1

Millichap JG, ‘Early-onset Epileptic Encephalopathies with Stxbpl Mutations’ (0AD) {volume} Pediatric Neurology Briefs {page} DOI: https://doi.org/10.15844/pedneurbriefs-24-12-1

[1]J. G. Millichap, “Early-Onset Epileptic Encephalopathies with STXBPl Mutations”, Pediatric Neurology Briefs, vol. {volume}, no. {issue}, p. {page}, 0AD, doi: 10.15844/pedneurbriefs-24-12-1.

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Epileptic Encephalopathies

Early-Onset Epileptic Encephalopathies with STXBPl Mutations

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Abstract

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