The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

BACKGROUND: Reading disability (RD) is a common neurodevelopmental disorder with genetic basis established in families segregating “pure” dyslexia. RD commonly occurs in neurodevelopmental disorders including Rolandic Epilepsy (RE), a complex genetic disorder. We performed genomewide linkage analysi...

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Detalles Bibliográficos
Autores principales: Strug, Lisa J., Addis, Laura, Chiang, Theodore, Baskurt, Zeynep, Li, Weili, Clarke, Tara, Hardison, Huntley, Kugler, Steven L., Mandelbaum, David E., Novotny, Edward J., Wolf, Steven M., Pal, Deb K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399896/
https://www.ncbi.nlm.nih.gov/pubmed/22815793
http://dx.doi.org/10.1371/journal.pone.0040696

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399896/
https://www.ncbi.nlm.nih.gov/pubmed/22815793
http://dx.doi.org/10.1371/journal.pone.0040696

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