Medical genetics: advances in brief: Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

. 1992 Jun;29(6):439.

Medical genetics: advances in brief

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

PMCID: PMC1016004

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Medori R., Tritschler H. J., LeBlanc A., Villare F., Manetto V., Chen H. Y., Xue R., Leal S., Montagna P., Cortelli P. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med. 1992 Feb 13;326(7):444–449. doi: 10.1056/NEJM199202133260704. [DOI] [PMC free article] [PubMed] [Google Scholar]