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

On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.

Neuropathology : official journal of the Japanese Society of Neuropathology - 1 Aug 2006

Ishikawa Kinya, Mizusawa Hidehiro

Abstract excerpt

Autosomal dominant cerebellar ataxia (ADCA) is a group of heterogeneous conditions. More than 20 genes or gene loci have been identified that are responsible for ADCA. Although expansions of the trinucleotide (CAG) repeat that encode polyglutamine are known to cause some forms of ADCA, growing knowledge about the genetic basis of ADCA indicates that many subtypes of ADCA are caused by mutations other than the CAG...

Read the complete abstract on PubMed

Topics

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

Share to Cerebellar Ataxia
Share to Chromosomes, Human, Pair 16

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Dominant

Share to Immunohistochemistry

Share to Peptides

Share to Purkinje Cells

Share to Trinucleotide Repeat Expansion

Source

Identifiers

PMID: 16961073
DOI: 10.1111/j.1440-1789.2006.00719.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.PMID 16961073Read ↗

16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.Semantic proximity Read ↗

Genetic cerebellar ataxias.Semantic proximity Read ↗

Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families.Semantic proximity Read ↗

Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.Semantic proximity Read ↗

Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.Semantic proximity Read ↗

Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan.Semantic proximity Read ↗

The genetic nomenclature of recessive cerebellar ataxias.Semantic proximity Read ↗

Autosomal-dominant cerebellar ataxias.Semantic proximity Read ↗

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.Semantic proximity Read ↗

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.Semantic proximity Read ↗

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