Identification of NCAN as a candidate gene for developmental dyslexia

A whole-genome linkage analysis in a Finnish pedigree of eight cases with developmental dyslexia (DD) revealed several regions shared by the affected individuals. Analysis of coding variants from two affected individuals identified rs146011974G > A (Ala1039Thr), a rare variant within the NCAN gen...

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Detalles Bibliográficos
Autores principales: Einarsdottir, Elisabet, Peyrard-Janvid, Myriam, Darki, Fahimeh, Tuulari, Jetro J., Merisaari, Harri, Karlsson, Linnea, Scheinin, Noora M., Saunavaara, Jani, Parkkola, Riitta, Kantojärvi, Katri, Ämmälä, Antti-Jussi, Yiu-Lin Yu, Nancy, Matsson, Hans, Nopola-Hemmi, Jaana, Karlsson, Hasse, Paunio, Tiina, Klingberg, Torkel, Leinonen, Eira, Kere, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570950/
https://www.ncbi.nlm.nih.gov/pubmed/28839234
http://dx.doi.org/10.1038/s41598-017-10175-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570950/
https://www.ncbi.nlm.nih.gov/pubmed/28839234
http://dx.doi.org/10.1038/s41598-017-10175-7

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