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Article

The Nuclear Factor κB–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

6 Jun 2007

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 17564964
DOI: 10.1086/518900

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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.

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The Nuclear Factor κB–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood OnsetPMID 17564964Read ↗

PLEKHG5-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nerves.Semantic proximity Read ↗

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Homozygous N-terminal missense variant in PLEKHG5 associated with intermediate CMT: A case report.Semantic proximity Read ↗

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Activation of a Potassium Channel Mutation That Causes Spinocerebellar Ataxia Promotes Aggregation of the RhoGEF Domain-Containing Protein Plekhg4.Semantic proximity Read ↗

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