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

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

19 May 2003

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 Lysosomal Storage Disorders Research
Share to Neurological diseases and metabolism
Share to Parkinson's Disease Mechanisms and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12781588
DOI: 10.1016/s1353-8020(03)00016-6

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological studyPMID 12781588Read ↗

Autosomal dominant parkinsonism: its etiologies and differential diagnoses.Semantic proximity Read ↗

Autosomal recessive parkinsonism.Semantic proximity Read ↗

PINK1 mutations and parkinsonism.Semantic proximity Read ↗

The Parkinson's disease-related genes act in mitochondrial homeostasisSemantic proximity Read ↗

A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.Semantic proximity Read ↗

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

LRRK2 R1441C mutation causing Parkinson's Disease in an Egyptian family.Semantic proximity Read ↗

Parkinson's disease and mitochondrial gene variations: a review.Semantic proximity Read ↗

Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism.Semantic proximity Read ↗

The Genetic Architecture of Parkinson's Disease in Morocco: Highlighting a Predominance of Mendelian Genes.Semantic proximity Read ↗

[The genetics of Parkinson syndrome].Semantic proximity Read ↗

Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's diseaseSemantic proximity Read ↗

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