A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment

Find Full text
Thumbnail
Fulltext:
150754.pdf
Embargo:
until further notice
Size:
1.909Mb
Format:
PDF
Description:
Publisher’s version
Publication year
2015
Author(s)
Lozano, R.
Vino, A.
Lozano, C.
Fisher, S.E.
Deriziotis, P.
Source
European Journal of Human Genetics, 23, 12, (2015), pp. 1702-1707
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/150754   https://hdl.handle.net/2066/150754
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.