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Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

Context: Dyslexia is a common disorder with a strong genetic component, but despite significant research effort, the aetiology is still largely unknown. Objective: To identify loci contributing to dyslexia risk. Methods: This was a genomewide linkage analysis in a single large family. Dutch families...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: de Kovel, C G F, Hol, F, Heister, J, Willemen, J, Sandkuijl, L, Franke, B, Padberg, G
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Group 2004
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735895/
https://ncbi.nlm.nih.gov/pubmed/15342694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2003.012294
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