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:	McCombie, W. Richard
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:	Publisher
URI:	https://repository.cshl.edu/id/eprint/28202

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