TY  -  
T1  - Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family 
SN  -  /  
UR  - http://hdl.handle.net/10138/203377 
T3  -  
A1  - Einarsdottir, Elisabet; Svensson, Idor; Darki, Fahimeh; Peyrard-Janvid, Myriam; Lindvall, Jessica M.; Ameur, Adam; Jacobsson, Christer; Klingberg, Torkel; Kere, Juha; Matsson, Hans 
A2  -  
PB  -  
Y1  - 2015 
LA  - eng 
AB  - 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 current study was to perform exome sequencing of affected and unaffected individuals within an extended pedigree with a familial form of developmental dyslexia. We identified a two-base mutation, causi... 
VO  -  
IS  -  
SP  -  
OP  -  
KW  - READING-DISABILITY; PROTEIN; CENTROSOME; GENES; DCDC2; GENETICS; COMPLEX; LINKAGE; DYX1C1; PREVALENCE; 3111 Biomedicine 
N1  -   
PP  -  
ER  -