Nonsyndromic intellectual disability with novel heterozygous SCN2A mutation and epilepsy
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2054-345X
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Nonsyndromic intellectual disability with novel heterozygous SCN2A mutation and epilepsy ; volume:5 ; number:1 ; day:20 ; month:7 ; year:2018 ; pages:1-3 ; date:12.2018
Human genome variation ; 5, Heft 1 (20.7.2018), 1-3, 12.2018
- Urheber
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Yokoi, Takayuki
- Beteiligte Personen und Organisationen
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Enomoto, Yumi
Tsurusaki, Yoshinori
Naruto, Takuya
Kurosawa, Kenji
SpringerLink (Online service)
- DOI
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10.1038/s41439-018-0019-5
- URN
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urn:nbn:de:101:1-2018092321115233358913
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:20 MESZ
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Beteiligte
- Yokoi, Takayuki
- Enomoto, Yumi
- Tsurusaki, Yoshinori
- Naruto, Takuya
- Kurosawa, Kenji
- SpringerLink (Online service)
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