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Article

A family with Parkinson disease, essential tremor, bell palsy, and parkin mutations.

Archives of neurology - 1 Mar 2007

Deng Hao, Le Wei-Dong, Hunter Christine B, Mejia Nicte, Xie Wen-Jie, Jankovic Joseph

Abstract excerpt

BACKGROUND: Mutations in the parkin gene cause autosomal recessive early-onset Parkinson disease (EOPD). The A265G variant in the HS1 binding protein 3 gene (HS1BP3) is common in essential tremor (ET). OBJECTIVE: To investigate the presence of mutations in the parkin gene and the A265G variant in...

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Identifiers

PMID: 17353387
DOI: 10.1001/archneur.64.3.421

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17353387-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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