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

Distribution of the B33 CTG repeat polymorphism in a subtype of schizophrenia.

European archives of psychiatry and clinical neuroscience - 1 Jan 1998

Bengel D, Balling U, Stöber G, Heils A, Li S H, Ross C A, Jungkunz G, Franzek E, Beckmann H, Riederer P, Lesch K P

Abstract excerpt

Clinical evidence for a dominant mode of inheritance and anticipation in periodic catatonia, a distinct subtype of schizophrenia, suggests that trinucleotide repeat expansions may be involved in the aetiology of this disorder. Since genes with triplet repeats are putative canditates for causing schizophrenia, we have analysed the polymorphic B33 CTG repeat locus on chromosome 3 in 45 patients with periodic...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Aged

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

Share to Chromosomes, Human, Pair 3

Share to Genes, Dominant

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Polymorphism, Genetic

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 9684916
DOI: 10.1007/s004060050021

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Distribution of the B33 CTG repeat polymorphism in a subtype of schizophrenia.PMID 9684916Read ↗

Triplet repeats in clinical subtypes of schizophrenia: variation at the DRPLA (B 37 CAG repeat) locus is not associated with periodic catatonia.Semantic proximity Read ↗

Genetic predisposition and environmental causes in periodic and systematic catatonia.Semantic proximity Read ↗

Genetic heterogeneity in catatonic schizophrenia: A family studySemantic proximity Read ↗

hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.Semantic proximity Read ↗

Exclusion of five trinucleotide repeat (CAG and CCG) expansions in 17 families with schizophrenia.Semantic proximity Read ↗

MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia.Semantic proximity Read ↗

Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder.Semantic proximity Read ↗

Support for "Disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia.Semantic proximity Read ↗

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.Semantic proximity Read ↗

Novel CAG/CTG repeat expansion mutations do not contribute to the genetic risk for most cases of bipolar disorder or schizophrenia.Semantic proximity Read ↗

Long repeat tracts at SCA8 in major psychosis.Semantic proximity Read ↗

Search for unstable DNA in schizophrenia families with evidence for genetic anticipation.Semantic proximity Read ↗

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