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Article

Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation.

European journal of pediatrics - 1 May 2005

Wohlrab Gabriele, Uyanik Goekhan, Gross Claudia, Hehr Ute, Winkler Jürgen, Schmitt Bernhard, Boltshauser Eugen

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Source

Identifiers

PMID: 15726411
DOI: 10.1007/s00431-005-1622-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation.PMID 15726411Read ↗

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.Semantic proximity Read ↗

The aristaless (Arx) gene: one gene for many "interneuronopathies".Semantic proximity Read ↗

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX.Semantic proximity Read ↗

Distinct DNA binding and transcriptional repression characteristics related to different ARX mutations.Semantic proximity Read ↗

Homeobox genes and human genetic disorders.Semantic proximity Read ↗

ARX spectrum disorders: making inroads into the molecular pathology.Semantic proximity Read ↗

The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes.Semantic proximity Read ↗

[Dysmorphic syndromes and regulatory genes].Semantic proximity Read ↗

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