CDKL5 deficiency disorder: At the intersection between Rett syndrome and developmental epileptic encephalopathies

This commentary is on the original articles by Wong et al. and Daniels et al. on pages 469–482 and 456–468 of this issue.

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Bibliographische Detailangaben
Veröffentlicht in:	Developmental medicine and child neurology Jg. 66; H. 4; S. 410 - 411
1. Verfasser:	Kaufmann, Walter E.
Format:	Journal Article
Sprache:	Englisch
Veröffentlicht:	England 01.04.2024
Schlagworte:	Epilepsy - genetics Epileptic Syndromes - genetics Humans Mutation - genetics Protein Serine-Threonine Kinases - genetics Rett Syndrome - complications Rett Syndrome - genetics Spasms, Infantile - genetics
ISSN:	0012-1622, 1469-8749, 1469-8749
Online-Zugang:	Volltext
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Beschreibung
Zusammenfassung:	This commentary is on the original articles by Wong et al. and Daniels et al. on pages 469–482 and 456–468 of this issue.
Bibliographie:	469–482 This commentary is on the original articles by Wong et al. and Daniels et al. on pages 456–468 of this issue. and ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0012-1622 1469-8749 1469-8749
DOI:	10.1111/dmcn.15797