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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 Onset

6 Jun 2007

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Amyotrophic Lateral Sclerosis Research
NF-κB Signaling Pathways
Signaling Pathways in Disease

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 17564964
DOI: 10.1086/518900

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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 ↗

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5Semantic proximity Read ↗

Novel mutation in KIF5A gene associated with hereditary motor and sensory neuropathy and cognitive impairment: a case report and literature review.Semantic proximity Read ↗

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