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Article

Shining a light on CNTNAP2: complex functions to complex disorders.

European journal of human genetics : EJHG - 1 Feb 2014

Rodenas-Cuadrado Pedro, Ho Joses, Vernes Sonja C

Abstract excerpt

The genetic basis of complex neurological disorders involving language are poorly understood, partly due to the multiple additive genetic risk factors that are thought to be responsible. Furthermore, these conditions are often syndromic in that they have a range of endophenotypes that may be associated with the disorder and that may be present in different combinations in patients. However, the emergence of...

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Amino Acid Sequence
Language Development Disorders
Membrane Proteins
Mutation, Missense
Nerve Net

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Nerve Tissue Proteins

Nervous System Diseases

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Open in PubMed Open full text

Identifiers

PMID: 23714751
DOI: 10.1038/ejhg.2013.100
PMCID: PMC3895625

Genes

CNTNAP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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Shining a light on CNTNAP2: complex functions to complex disorders.PMID 23714751Read ↗

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