Nonsyndromic intellectual disability with novel heterozygous SCN2A mutation and epilepsy

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2054-345X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Creator: Yokoi, Takayuki

Contributor: Enomoto, Yumi
Tsurusaki, Yoshinori
Naruto, Takuya
Kurosawa, Kenji
SpringerLink (Online service)

DOI: 10.1038/s41439-018-0019-5

URN: urn:nbn:de:101:1-2018092321115233358913

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:20 AM CEST

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Yokoi, Takayuki
Enomoto, Yumi
Tsurusaki, Yoshinori
Naruto, Takuya
Kurosawa, Kenji
SpringerLink (Online service)

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Nonsyndromic intellectual disability with novel heterozygous SCN2A mutation and epilepsy

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Other Objects (12)

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