Phenotypic expansion of EGP5-related Vici syndrome: 15 Dutch patients carrying a founder variant.

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Bibliographic Details
Title: Phenotypic expansion of EGP5-related Vici syndrome: 15 Dutch patients carrying a founder variant.
Authors: Vansenne F; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands. Electronic address: f.vansenne@umcg.nl., Fock JM; Department of Pediatric Neurology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Stolte-Dijkstra I; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Meiners LC; Department of Radiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., van den Boogaard MH; Department of Genetics, University Medical Center Utrecht, University of Utrecht, Utrecht, the Netherlands., Jaeger B; Department of Pediatric Neurology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands., Boven L; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Vos YJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Sinke RJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Verbeek DS; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Source: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society [Eur J Paediatr Neurol] 2022 Nov; Vol. 41, pp. 91-98. Date of Electronic Publication: 2022 Nov 12.
Publication Type: Journal Article
Journal Info: Publisher: Saunders Country of Publication: England NLM ID: 9715169 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2130 (Electronic) Linking ISSN: 10903798 NLM ISO Abbreviation: Eur J Paediatr Neurol Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1532-2130
DOI:10.1016/j.ejpn.2022.11.003