The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.
<h4>Background</h4>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 perform...
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| Auteurs principaux: | , , , , , , , , , , , |
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| Format: | article |
| Langue: | EN |
| Publié: |
Public Library of Science (PLoS)
2012
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| Accès en ligne: | https://doaj.org/article/abfb5ed79ddd4be28e2b968ea47c8eab |
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