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

A Microdeletion of D6S305 in a Family of Autosomal Recessive Juvenile Parkinsonism (PARK2)

1 Apr 1998

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 Neurological diseases and metabolism
Share to Nuclear Receptors and Signaling
Share to Parkinson's Disease Mechanisms and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9570960
DOI: 10.1006/geno.1997.5196

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Microdeletion of D6S305 in a Family of Autosomal Recessive Juvenile Parkinsonism (PARK2)PMID 9570960Read ↗

PARK2 Microdeletion or Duplications Have Been Implicated in Different Neurological Disorders Including Early Onset Parkinson DiseaseSemantic proximity Read ↗

ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease.Semantic proximity Read ↗

DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability.Semantic proximity Read ↗

Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutationSemantic proximity Read ↗

Novel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification.Semantic proximity Read ↗

Pseudo-heterozygous rearrangement mutation of parkin.Semantic proximity Read ↗

Rapid identification of disease-causing mutations using copy number analysis within linkage intervals.Semantic proximity Read ↗

Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease.Semantic proximity Read ↗

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.Semantic proximity Read ↗

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

A novel genomic mutation in ADNP leading to intellectual disability.Semantic proximity Read ↗

Levodopa-responsive dystonia caused by biallelic PRKN exon inversion invisible to exome sequencingSemantic proximity Read ↗

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