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Presenting the diagnosis of pseudoseizure

1 May 1990

Abstract excerpt

Mutations in parkin and PTEN-induced protein kinase (PINK1) represent the two most common causes of autosomal recessive parkinsonism. The possibility that heterozygous mutations in these genes also predispose to disease, or lower the age of disease onset, has been suggested, but currently there is insufficient data to conclusively verify this hypothesis. <b>Objective:</b> To study the frequency and spectrum of...

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PMID: 2330101
DOI: 10.1212/wnl.40.5.756

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