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Article

Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testis.

Journal of human genetics - 1 Jan 2003

Zeng Li, Gu Shaohua, Li Yao, Zhao Enpeng, Xu Jian, Ye Xin, Wu Qinhan, Wang Liu, Xie Yi, Mao Yumin

Abstract excerpt

Mutations in the X-linked gene doublecortex (DCX) result in lissencephaly in males or subcortical laminar heterotopia (double cortex) in females. Recently, an evolutionarily conserved doublecortin (DC) domain important for microtubule binding and microtubule polymerization was defined according t...

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Source

Identifiers

PMID: 12820024
DOI: 10.1007/s10038-003-0033-3

Genes

DCDC1
DCX

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12820024-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

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Research trail→

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Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testis.PMID 12820024Read ↗

Doublecortin mutations cluster in evolutionarily conserved functional domains.Semantic proximity Read ↗

A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.Semantic proximity Read ↗

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.Semantic proximity Read ↗

Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother.Semantic proximity Read ↗

New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.Semantic proximity Read ↗

Familial pachygyria in both genders related to a DCX mutation.Semantic proximity Read ↗

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.Semantic proximity Read ↗

Genes that regulate neuronal migration in the cerebral cortex.Semantic proximity Read ↗

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.Semantic proximity Read ↗

Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.Semantic proximity Read ↗

Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing.Semantic proximity Read ↗

The location of DCX mutations predicts malformation severity in X-linked lissencephaly.Semantic proximity Read ↗

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