Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1866-1955

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Functional characterization of rare FOXP2 variants in neurodevelopmental disorder ; volume:8 ; number:1 ; day:28 ; month:11 ; year:2016 ; pages:1-19 ; date:12.2016
Journal of neurodevelopmental disorders ; 8, Heft 1 (28.11.2016), 1-19, 12.2016

Keyword: Kardiovaskuläre Krankheit

Creator: Estruch, Sara B.

Contributor: Graham, Sarah A.
Chinnappa, Swathi M.
Deriziotis, Pelagia
Fisher, Simon E.
SpringerLink (Online service)

DOI: 10.1186/s11689-016-9177-2

URN: urn:nbn:de:1111-201701137931

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:00 AM CEST

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Estruch, Sara B.
Graham, Sarah A.
Chinnappa, Swathi M.
Deriziotis, Pelagia
Fisher, Simon E.
SpringerLink (Online service)

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Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

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Other Objects (12)

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Rare mosaic variant of GJA1 in a patient with a neurodevelopmental disorder

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