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Article

A Novel Nonsense Mutation in SCN9A in a Moroccan Child With Congenital Insensitivity to Pain

12 Jul 2014

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Share to Hereditary Neurological Disorders
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 25439579
DOI: 10.1016/j.pediatrneurol.2014.06.009

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Novel Nonsense Mutation in SCN9A in a Moroccan Child With Congenital Insensitivity to PainPMID 25439579Read ↗

A novel mutation in SCN9A in a child with congenital insensitivity to pain.Semantic proximity Read ↗

[Congenital insensitivity to pain caused by a novel SCN9A-genotype].Semantic proximity Read ↗

Novel SCN9A missense mutations contribute to congenital insensitivity to pain: Unexpected correlation between electrophysiological characterization and clinical phenotype.Semantic proximity Read ↗

Novel SCN9A variant associated with congenital insensitivity to pain.Semantic proximity Read ↗

A Novel Homozygous Pathogenic Variant in SCN9A Gene Causing Hereditary Sensory and Autonomic Neuropathy Type ID: A Case ReportSemantic proximity Read ↗

[Novel compound heterozygous SCN9A variations causing congenital insensitivity to pain in a patient].Semantic proximity Read ↗

A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia.Semantic proximity Read ↗

An SCN9A channelopathy causes congenital inability to experience pain.Semantic proximity Read ↗

Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A.Semantic proximity Read ↗

Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutationsSemantic proximity Read ↗

Novel SCN9A variant associated with congenital insensitivity to pain.Semantic proximity Read ↗

A stop codon mutation in SCN9A causes lack of pain sensation.Semantic proximity Read ↗

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