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Article

An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene.

Neurology - 10 Dec 2002

Broccolini A, Pescatori M, D'Amico A, Sabino A, Silvestri G, Ricci E, Servidei S, Tonali P A, Mirabella M

Abstract excerpt

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Topics

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Share to Carbohydrate Epimerases
Share to Chromosomes, Human, Pair 9
Share to Escherichia coli Proteins
Share to Genes, Recessive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscle, Skeletal

Share to Myositis, Inclusion Body

Share to Reverse Transcriptase Polymerase Chain Reaction

Source

Identifiers

PMID: 12473780
DOI: 10.1212/01.wnl.0000031808.04545.e0

Genes

GNE

Provenance

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

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Semantic proximity does not establish scientific evidence.

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Two recurrent mutations are associated with GNE myopathy in the North of Britain.Semantic proximity Read ↗

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