Molecular characterisation of rare loss-of-function NPAS3 and NPAS4 variants identified in individuals with neurodevelopmental disorders

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Molecular characterisation of rare loss-of-function NPAS3 and NPAS4 variants identified in individuals with neurodevelopmental disorders ; volume:11 ; number:1 ; day:23 ; month:3 ; year:2021 ; pages:1-11 ; date:12.2021
Scientific reports ; 11, Heft 1 (23.3.2021), 1-11, 12.2021

Creator: Rossi, Joseph J.
Rosenfeld, Jill A.
Chan, Katie M.
Streff, Haley
Nankivell, Victoria
Peet, Daniel J.
Whitelaw, Murray L.
Bersten, David C.

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-021-86041-4

URN: urn:nbn:de:101:1-2022111421330504086912

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:29 AM CEST

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Rossi, Joseph J.
Rosenfeld, Jill A.
Chan, Katie M.
Streff, Haley
Nankivell, Victoria
Peet, Daniel J.
Whitelaw, Murray L.
Bersten, David C.
SpringerLink (Online service)

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Molecular characterisation of rare loss-of-function NPAS3 and NPAS4 variants identified in individuals with neurodevelopmental disorders

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Other Objects (12)

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ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants

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Tspyl2 Loss-of-Function Causes Neurodevelopmental Brain and Behavior Abnormalities in Mice

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