Work

Fatal familial insomnia: A second kindred with mutation of prion protein gene at codon 178

Year: 1992

Type: article

Source: Neurology

DOI: 10.1212/wnl.42.3.669

Authors: R. Medori, P. Montagna, H. J. Tritschler, A. LeBlanc, P. Cortelli, P. Tinuper, E. Lugaresi, P. Gambetti

Institutions: Case Western Reserve University, University of Bologna, Istituto delle Scienze Neurologiche di Bologna

Language: English

Topic: Prion Diseases and Protein Misfolding

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institute on Aging, National Human Genome Research Institute, National Institute of Neurological Disorders and Stroke

Awards: G3019247282, UHC/CWRU ALZHEIMER'S DISEASE RESEARCH CENTER, G3725295595, SYNAPTOSOMES AND AXONS, G5606450302, UW Center for Mendelian Genomics

OpenAlex ID: W2002709428

FWCI: 5.587

Cites:

Cited by: 209

Related to: 10