Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

Dyslexia is a common heritable developmental disorder involving impaired reading abilities. Its genetic underpinnings are thought to be complex and heterogeneous, involving common and rare genetic variation. Multigenerational families segregating apparent monogenic forms of language-related disorder...

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Detalles Bibliográficos
Autores principales: Carrion-Castillo, Amaia, Estruch, Sara B., Maassen, Ben, Franke, Barbara, Francks, Clyde, Fisher, Simon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263547/
https://www.ncbi.nlm.nih.gov/pubmed/34076780
http://dx.doi.org/10.1007/s00439-021-02289-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263547/
https://www.ncbi.nlm.nih.gov/pubmed/34076780
http://dx.doi.org/10.1007/s00439-021-02289-w

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