Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family

Developmental dyslexia is the most common learning disorder in children. Problems in reading and writing are likely due to a complex interaction of genetic and environmental factors, resulting in reduced power of studies of the genetic factors underlying developmental dyslexia. Our approach in the c...

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Dades bibliogràfiques
Publicat a:Hum Genet
Autors principals: Einarsdottir, Elisabet, Svensson, Idor, Darki, Fahimeh, Peyrard-Janvid, Myriam, Lindvall, Jessica M., Ameur, Adam, Jacobsson, Christer, Klingberg, Torkel, Kere, Juha, Matsson, Hans
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2015
Matèries:
Original Investigation
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4628622/
https://ncbi.nlm.nih.gov/pubmed/26400686
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-015-1602-1
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