Family-based association study of DYX1C1 variants in autism.

doi:10.1038/sj.ejhg.5201272

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Article

Family-based association study of DYX1C1 variants in autism.

European journal of human genetics : EJHG - 1 Jan 2005

Ylisaukko-Oja Tero, Peyrard-Janvid Myriam, Lindgren Cecilia M, Rehnström Karola, Vanhala Raija, Peltonen Leena, Järvelä Irma, Kere Juha

Abstract excerpt

DYX1C1: was recently identified as a candidate gene for developmental dyslexia, which is characterized by an unexpected difficulty in learning to read and write despite adequate intelligence, motivation, and education. It will be important to clarify, whether the phenotype caused by DYX1C1 extends to other language-related or comorbid disorders. Impaired language development is one of the essential features in...

Topics

Alleles
Autistic Disorder
Cytoskeletal Proteins
Family
Female
Genetic Markers
Genetic Predisposition to Disease
Genotype
Haplotypes
Humans
Linkage Disequilibrium
Male
Nerve Tissue Proteins
Nuclear Proteins
Polymorphism, Single Nucleotide

Source

Open in PubMed

Identifiers

PMID: 15470369
DOI: 10.1038/sj.ejhg.5201272

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