A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Hum Genet
Main Authors: Einarsdottir, Elisabet, Svensson, Idor, Darki, Fahimeh, Peyrard-Janvid, Myriam, Lindvall, Jessica M., Ameur, Adam, Jacobsson, Christer, Klingberg, Torkel, Kere, Juha, Matsson, Hans
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2015
Assuntos:
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!