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Article

Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism.

BMC neurology - 16 Dec 2008

Myhre Ronny, Steinkjer Stina, Stormyr Alice, Nilsen Gina L, Abu Zayyad Hiba, Horany Khalid, Nusier Mohamad K, Klungland Helge

Abstract excerpt

BACKGROUND: Parkinson's disease is a progressive neurodegenerative disorder, where most cases are sporadic with a late onset. In rare incidences familial forms of early-onset parkinsonism occur, and when recessively inherited, cases are often explained by mutations in either the parkin (PARK2) or...

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Source

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Identifiers

PMID: 19087301
DOI: 10.1186/1471-2377-8-47
PMCID: PMC2635385

Genes

PINK1
PARK7

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19087301-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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