Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families [29]

Nieto, A., Goldfarb, L. G., Brown, P., McCombie, W. R., Trapp, S., Asher, D. M., Gajdusek, D. C. (1991) Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families [29]. Lancet, 337 (8741). pp. 622-623. ISSN 01406736 (ISSN)

URL: http://www.ncbi.nlm.nih.gov/pubmed/1671983
DOI: 10.1016/0140-6736(91)91696-R
Item Type: Paper
Uncontrolled Keywords: adult aged codon creutzfeldt jakob disease female genetic analysis human letter major clinical study male molecular genetics mutation priority journal Creutzfeldt-Jakob Syndrome France Hungary Middle Age Netherlands United States
Subjects: bioinformatics > genomics and proteomics > analysis and processing > codon processing
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification
diseases & disorders
bioinformatics > genomics and proteomics > genetics & nucleic acid processing
bioinformatics > genomics and proteomics
diseases & disorders > mental disorders > genetic disorders
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > mutations
CSHL Authors:
Communities: CSHL labs > McCombie lab
Depositing User: Matt Covey
Date: 1991
Date Deposited: 25 Apr 2013 18:02
Last Modified: 25 Apr 2013 18:02
Related URLs:
URI: https://repository.cshl.edu/id/eprint/28202

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