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Article

Broadening the clinical spectrum of FUS mutations: a case with monomelic amyotrophy with a late progression to amyotrophic lateral sclerosis.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Mar 2021

Moglia Cristina, Calvo Andrea, Brunetti Maura, Chiò Adriano, Grassano Maurizio

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Share to Amyotrophic Lateral Sclerosis
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Share to RNA-Binding Protein FUS

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

Share to Spinal Muscular Atrophies of Childhood

Source

Identifiers

PMID: 33001405
DOI: 10.1007/s10072-020-04751-5

Genes

FUS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Broadening the clinical spectrum of FUS mutations: a case with monomelic amyotrophy with a late progression to amyotrophic lateral sclerosis.PMID 33001405Read ↗

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Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation.Semantic proximity Read ↗

New advances in Amyotrophic Lateral Sclerosis genetics: Towards gene therapy opportunities for familial and young cases.Semantic proximity Read ↗

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