Persistent URL of this record https://hdl.handle.net/1887/116284
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Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders
- All authors
- Sollis, E.; Deriziotis, P.; Saitsu, H.; Miyake, N.; Matsumoto, N.; Hoffer, M.J.V.; Ruivenkamp, C.A.L.; Alders, M.; Okamoto, N.; Bijlsma, E.K.; Plomp, A.S.; Fisher, S.E.
- Date
- 2017-11-30
- Journal
- Human Mutation
- Volume
- 38
- Issue
- 11
- Pages
- 1542 - 1554