Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

Estruch, S. B., Graham, S. A., Chinnappa, S. M., Deriziotis, P., & Fisher, S. E. (2016). Functional characterization of rare FOXP2 variants in neurodevelopmental disorder. Journal of Neurodevelopmental Disorders, 8: 44. doi:10.1186/s11689-016-9177-2.
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01. DNA sequences of primers used for molecular cloning 02. DNA sequences of primers used for site-directed mutagenesis 03. Western blots of YFP-tagged FOXP2 variants 04. Summary of studies examining FOXP2 polyglutamine tract length variation in individuals with neurodevelopmental and … 05. FOXP2 polyglutamine tract lengths in selected vertebrates

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Journal article
Publication date
2016
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