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Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism
- Dr Nobuaki Wakamatsu, Department of Genetics, Institute for Developmental Research, Aichi Human Service Center, 713−8 Kamiya, Kasugai, Aichi 480−0392, Japan. Telephone 0081 568 88 0811; fax 0081 568 88 0829; email nwake{at}inst-hsc.pref.aichi.jp
Citation
Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism
Publication history
- Received November 5, 1998
- Revised February 8, 1999
- Accepted March 18, 1999
- First published August 1, 1999.
Online issue publication
April 13, 2016
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Journal of Neurology, Neurosurgery, and Psychiatry