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Article

One genetic mutation, two diseases: fatal familial insomnia and Creutzfeldt-Jakob disease.

Comprehensive therapy - 1 Jan 1993

Bellows J G

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PMID: 8334858

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Related research

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One genetic mutation, two diseases: fatal familial insomnia and Creutzfeldt-Jakob disease.PMID 8334858Read ↗

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Expert Consensus on Clinical Diagnostic Criteria for Fatal Familial Insomnia.Semantic proximity Read ↗

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Sporadic Creutzfeldt-Jakob disease: further twists and turns in a convoluted protein.Semantic proximity Read ↗

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