Lhermitte-Duclos disease with concomitant KCNT2 gene mutation: report of an extremely rare combination.

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Bibliographic Details
Title: Lhermitte-Duclos disease with concomitant KCNT2 gene mutation: report of an extremely rare combination.
Authors: Assi J; School of Medicine, Faculty of Health Sciences, Democritus University of Thrace, Alexandroupolis, Greece., Chyta M; School of Medicine, Faculty of Health Sciences, Democritus University of Thrace, Alexandroupolis, Greece., Mavridis I; School of Medicine, Faculty of Health Sciences, Democritus University of Thrace, Alexandroupolis, Greece. inmavridis@gmail.com.; Department of Neurosurgery, School of Medicine, Faculty of Health Sciences, Democritus University of Thrace, University General Hospital of Alexandroupolis, Alexandroupolis, Greece. inmavridis@gmail.com.
Source: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2023 Nov; Vol. 39 (11), pp. 3295-3299. Date of Electronic Publication: 2023 Jun 27.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8503227 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1433-0350 (Electronic) Linking ISSN: 02567040 NLM ISO Abbreviation: Childs Nerv Syst Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1433-0350
DOI:10.1007/s00381-023-06039-3