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Article

N98S mutation in NEFL gene is dominantly inherited with a phenotype of polyneuropathy and cerebellar atrophy.

Journal of the neurological sciences - 15 Jun 2016

Yang Yi, Gu Li-Qiang, Burnette William B, Li Jun

Abstract excerpt

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Topics

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Share to Atrophy
Share to Cerebellar Diseases
Share to Cerebellum
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Neurofilament Proteins

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Share to Polyneuropathies

Source

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Identifiers

PMID: 27206872
DOI: 10.1016/j.jns.2016.04.007
PMCID: PMC4877039

Genes

NEFL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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N98S mutation in NEFL gene is dominantly inherited with a phenotype of polyneuropathy and cerebellar atrophy.PMID 27206872Read ↗

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