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

The co‐occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome

10 Feb 2009

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 Cardiac Fibrosis and Remodeling
Share to Congenital heart defects research
Share to Tissue Engineering and Regenerative Medicine

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19208384
DOI: 10.1002/ajmg.a.32650

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The co‐occurrence of early onset Parkinson disease and 22q11.2 deletion syndromePMID 19208384Read ↗

Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.Semantic proximity Read ↗

Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessive.Semantic proximity Read ↗

Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence.Semantic proximity Read ↗

PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36Semantic proximity Read ↗

Chromosome 22q11.2 deletion may contain a locus for recessive early-onset Parkinson's disease.Semantic proximity Read ↗

Pure Parkinsonism as Possible Phenotype Expansion of THAP1-Related Disorders.Semantic proximity Read ↗

Childhood-Onset Schizophrenia Associated With Parkinsonism in a Patient With a Microdeletion of Chromosome 22Semantic proximity Read ↗

The genetics of autosomal recessive early-onset Parkinson's diseaseSemantic proximity Read ↗

A susceptibility locus for Parkinson's disease maps to chromosome 2p13Semantic proximity Read ↗

Parkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment.Semantic proximity Read ↗

Juvenile parkinsonism: Differential diagnosis, genetics, and treatmentSemantic proximity Read ↗

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.Semantic proximity Read ↗

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