Article info
PDFUnusual association of diseases/symptoms
CASE REPORT
Case of fatal familial insomnia caused by a d178n mutation with phenotypic similarity to Hashimoto’s encephalopathy
- Correspondence to Dr Gholam K Motamedi, motamedi{at}georgetown.edu
Citation
Case of fatal familial insomnia caused by a d178n mutation with phenotypic similarity to Hashimoto’s encephalopathy
Publication history
- Accepted June 20, 2018
- First published July 15, 2018.
Online issue publication
August 07, 2018
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© BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.