Rapid genome sequencing for infantile-onset epilepsy within a national health-care setting

dc.citation.epageLancet Neurol. 2024 Feb;23(2):139-140. doi: 10.1016/S1474-4422(23)00429-5.
dc.citation.issue2
dc.citation.spage139-140
dc.citation.volume23
dc.contributor.authorRobinson, H. K.
dc.contributor.authorStals, K.
dc.contributor.authorHill, S.
dc.contributor.authorParrish, A.
dc.contributor.authorBaple, E. L.
dc.date.accessioned2024-04-22T14:05:54Z
dc.date.available2024-04-22T14:05:54Z
dc.date.epub2024-01-25
dc.date.issued2024-02-01
dc.description.admin-noteunknown
dc.description.noteThe article is available via Open Access. Click on the 'Additional link' above to access the full-text.
dc.identifier.citationRobinson HK, Stals K, Hill S, Parrish A, Baple EL. Rapid genome sequencing for infantile-onset epilepsy within a national health-care setting. The Lancet Neurology. 2024;23(2):139-40.
dc.identifier.doi10.1016/s1474-4422(23)00429-5
dc.identifier.journalThe Lancet. Neurology
dc.identifier.pmid38267181
dc.identifier.urihttps://hdl.handle.net/11287/623222
dc.language.isoeng
dc.publisherElsevier
dc.relation.urlhttps://linkinghub.elsevier.com/retrieve/pii/S1474-4422(23)00429-5
dc.rights© 2023 Elsevier Ltd. All rights reserved.
dc.subjectHumans
dc.subjectInfant
dc.subject*Epilepsy/diagnosis/genetics
dc.subject*Spasms, Infantile
dc.subjectMutation
dc.titleRapid genome sequencing for infantile-onset epilepsy within a national health-care setting
dc.typeLetter
dc.type.versionppublish
Files