A search for a mutation in the tumour necrosis factor-alpha gene in narcolepsy

11Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The discovery of almost 100% association of narcolepsy with human leukocyte antigens (HLA) DR2 antigen prompted molecular biological research of this disorder. In the HLA class II gene cluster, the gene for tumour necrosis factor-alpha (TNF-α), which plays a role in the regulation of normal human sleep, is located. The present study searched for a mutation in the TNF-α gene by single-strand conformation polymorphism analysis (SSCP) in patients with narcolepsy. No mutation was detected in exons and introns of the TNF-α gene by SSCP and sequencing.

Cite

CITATION STYLE

APA

Kato, T., Honda, M., Kuwata, S., Juji, T., Fukuda, M., Honda, Y., & Kato, N. (1999). A search for a mutation in the tumour necrosis factor-alpha gene in narcolepsy. Psychiatry and Clinical Neurosciences, 53(3), 421–423. https://doi.org/10.1046/j.1440-1819.1999.00568.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free