Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in BUD13, a Component of the Retention and Splicing (RES) Complex

Specific language impairment (SLI) is a common neurodevelopmental disorder (NDD) that displays high heritability estimates. Genetic studies have identified several loci, but the molecular basis of SLI remains unclear. With the aim to better understand the genetic architecture of SLI, we performed wh...

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Detalles Bibliográficos
Autores principales: Andres, Erin M., Earnest, Kathleen Kelsey, Zhong, Cuncong, Rice, Mabel L., Raza, Muhammad Hashim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773923/
https://www.ncbi.nlm.nih.gov/pubmed/35053791
http://dx.doi.org/10.3390/brainsci12010047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773923/
https://www.ncbi.nlm.nih.gov/pubmed/35053791
http://dx.doi.org/10.3390/brainsci12010047

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