Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Stuttering and AP4E1[original query] |
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| Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering. American journal of human genetics 2015 Nov 97 (5): 715-25. Raza M Hashim, Mattera Rafael, Morell Robert, Sainz Eduardo, Rahn Rachel, Gutierrez Joanne, Paris Emily, Root Jessica, Solomon Beth, Brewer Carmen, Basra M Asim Raza, Khan Shaheen, Riazuddin Sheikh, Braun Allen, Bonifacino Juan S, Drayna Denn |
| Genetic factors and therapy outcomes in persistent developmental stuttering. Journal of communication disorders 2019 4 80 11-17. Frigerio-Domingues Carlos E, Gkalitsiou Zoi, Zezinka Alexandra, Sainz Eduardo, Gutierrez Joanne, Byrd Courtney, Webster Ronald, Drayna Denn |
| Neuroanatomical anomalies associated with rare AP4E1 mutations in people who stutter. Brain communications 2021 12 3 (4): fcab266. Chow Ho Ming, Li Hua, Liu Siyuan, Frigerio-Domingues Carlos, Drayna Denn |
| Genetic analyses of a large consanguineous south Indian family reveal novel variants in NAGPA and four hitherto unreported genes in developmental stuttering. Annals of human genetics 2024 10 . G Nandhini Devi, Navneesh Yadav, Chandru Jayashankaran, Jeffrey Justin Margret, Mathuravalli Krishnamoorthy, Sorna Lakshmi A, Chandralekha Meenakshi Sundaram, N P Karthikeyan, B K Thelma, C R Srikumari Srisailapat |
- Page last reviewed:Feb 1, 2024
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