Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Late-onset hereditary spastic paraplegia associated with a genetic variant in interferon induced with helicase c domain 1 (IFIH1) gene.

QJM : monthly journal of the Association of Physicians - 28 Jul 2023

Zhang S-Y, Zhu L, Fan L-L, Xiang R, Zeng L, Jin J-Y

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Interferon-Induced Helicase, IFIH1
Share to Interferons
Share to Mutation
Share to Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Spastic Paraplegia, Hereditary

Source

Identifiers

PMID: 37040079
DOI: 10.1093/qjmed/hcad055

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Late-onset hereditary spastic paraplegia associated with a genetic variant in interferon induced with helicase c domain 1 (IFIH1) gene.PMID 37040079Read ↗

Adult-onset severe methylenetetrahydrofolate reductase deficiency characterized by reversible spastic paraplegia with a novel mutation.Semantic proximity Read ↗

Mutations in ADAR1, IFIH1, and RNASEH2B presenting as spastic paraplegia.Semantic proximity Read ↗

Brief Report: IFIH1 Mutation Causes Systemic Lupus Erythematosus With Selective IgA DeficiencySemantic proximity Read ↗

Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxia.Semantic proximity Read ↗

HSP60 is a rare cause of hereditary spastic paraparesis, but may act as a genetic modifier.Semantic proximity Read ↗

Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.Semantic proximity Read ↗

Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation.Semantic proximity Read ↗

A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation.Semantic proximity Read ↗

Neurological Findings and a Brief Review of the Current Literature in a Severe Case of Aicardi-Goutières Syndrome Due to an IFIH1 Mutation.Semantic proximity Read ↗

Early-onset hereditary spastic paraplegia: the possibility of a genetic diagnosis.Semantic proximity Read ↗

Illustration of a rare case of hereditary spastic paraplegia type 30 associated with a missense variant in the non-motor domain of KIF1A.Semantic proximity Read ↗

HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.