In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

Thumbnail
Fulltext:
288487.pdf
Size:
701.4Kb
Format:
PDF
Description:
Publisher’s version
Download
Publication year
2022
Author(s)
Morison, L.D.
Meffert, E.
Stampfer, M.
Koolen, D.A.
Kleefstra, T.
Fisher, S.E.
et al.
Source
Journal of Medical Genetics, 0, (2022), pp. 1-11
ISSN
DOI
Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/288487   https://hdl.handle.net/2066/288487
Display more details

Upload full text

Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.