Severe childhood speech disorder
Gene discovery highlights transcriptional dysregulation
Abstract
Objective
Methods
Results
Conclusion
Related Infographic
Get full access to this article
View all available purchase options and get full access to this article.
References
Information & Authors
Information
Published In
Copyright
Publication History
Disclosure
Study Funding
Authors
Metrics & Citations
Metrics
Citation information is sourced from Crossref Cited-by service.
Citations
If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Select your manager software from the list below and click Download.
- Expanding the molecular landscape of childhood apraxia of speech: evidence from a single-center experience, Frontiers in Neuroscience, 18, (2024).https://doi.org/10.3389/fnins.2024.1396240
- The Schwann cell-specific G-protein Gαo (Gnao1) is a cell-intrinsic controller contributing to the regulation of myelination in peripheral nerve system, Acta Neuropathologica Communications, 12, 1, (2024).https://doi.org/10.1186/s40478-024-01720-3
- Genome Sequencing of Idiopathic Speech Delay, Human Mutation, 2024, (1-14), (2024).https://doi.org/10.1155/2024/9692863
- DDX3X syndrome: From clinical phenotypes to biological insights , Journal of Neurochemistry, (2024).https://doi.org/10.1111/jnc.16174
- GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity , Clinical Obesity, 14, 4, (2024).https://doi.org/10.1111/cob.12661
- The clinical and genetic spectrum of paediatric speech and language disorders, Brain, (2024).https://doi.org/10.1093/brain/awae264
- Deficiency of DDX3X results in neurogenesis defects and abnormal behaviors via dysfunction of the Notch signaling , Proceedings of the National Academy of Sciences, 121, 45, (2024).https://doi.org/10.1073/pnas.2404173121
- An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech, Journal of Speech, Language, and Hearing Research, 67, 9S, (3437-3451), (2024).https://doi.org/10.1044/2023_JSLHR-22-00714
- Multi-omics analysis detail a submicroscopic inv(15)(q14q15) generating fusion transcripts and MEIS2 and NUSAP1 haploinsufficiency, Scientific Reports, 14, 1, (2024).https://doi.org/10.1038/s41598-024-81507-7
- Expression and regulation of SETBP1 in the song system of male zebra finches (Taeniopygia guttata) during singing, Scientific Reports, 14, 1, (2024).https://doi.org/10.1038/s41598-024-75353-w
- See more
View Options
Login options
Check if you have access through your login credentials or your institution to get full access on this article.
Personal login Institutional LoginPurchase Options
The neurology.org payment platform is currently offline. Our technical team is working as quickly as possible to restore service.
If you need immediate support or to place an order, please call or email customer service:
- 1-800-638-3030 for U.S. customers - 8:30 - 7 pm ET (M-F)
- 1-301-223-2300 for customers outside the U.S. - 8:30 - 7 pm ET (M-F)
- [email protected]
We appreciate your patience during this time and apologize for any inconvenience.