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

AMACR mutations cause late-onset autosomal recessive cerebellar ataxia.

Neurology - 17 May 2011

Dick David, Horvath Rita, Chinnery Patrick F

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 Epilepsy, Tonic-Clonic
Share to Gait Disorders, Neurologic
Share to Memory Disorders
Share to Neurologic Examination

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neuropsychological Tests

Share to Racemases and Epimerases

Share to Speech Disorders

Share to Spinocerebellar Degenerations

Source

Open in PubMed Open full text

Identifiers

PMID: 21576695
DOI: 10.1212/WNL.0b013e31821a4484
PMCID: PMC3100132

Genes

AMACR

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

AMACR mutations cause late-onset autosomal recessive cerebellar ataxia.PMID 21576695Read ↗

Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations.Semantic proximity Read ↗

Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene.Semantic proximity Read ↗

New autosomal recessive cerebellar ataxias with oculomotor apraxia.Semantic proximity Read ↗

FMR1 premutation as a rare cause of late onset ataxiaSemantic proximity Read ↗

Homozygosity for c 6325T>G transition in the ATM gene causes an atypical, late-onset variant form of ataxia-telangiectasia.Semantic proximity Read ↗

Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA.Semantic proximity Read ↗

Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G MutationsSemantic proximity Read ↗

Early-Onset Cerebellar Atrophy Associated With Mutation in the CACNA1A GeneSemantic proximity Read ↗

ARV1 Gene: A Novel Cause of Autosomal Recessive Cerebellar Ataxia with Elevated Alpha FetoproteinSemantic proximity Read ↗

A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA.Semantic proximity Read ↗

Heterozygous Deletion of KLHL1/ATX8OS at the SCA8 Locus Is Unlikely Associated With Cerebellar Impairment in Humans.Semantic proximity Read ↗

Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.Semantic proximity Read ↗

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