No detectable mutations at Werner helicase locus in progeria [15]

Lancet

Volumn 348, Issue 9034, 1996, Pages 1106-

  Oshima, J ^a   Brown, W T ^a   Martin, G M ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE;

ADOLESCENT; CHILD; CLINICAL ARTICLE; FEMALE; HUMAN; LETTER; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGERIA; SCHOOL CHILD; WERNER SYNDROME;

EID: 0029808588     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)64456-X     Document Type: Letter

References (5)

1. GM Martin CA Sprague CJ Epstein Replicative life-span of cultivated human cells: effects of donor's age, tissue and genotype Lab Invest 23 1970 86 92
2. WT Brown Genetic diseases of premature aging as models of senescence Annu Rev Gerontol Geriatr 10 1990 23 42
3. CE Yu J Oshima YH Fu Positional cloning of the Werner's syndrome gene Science 272 1996 258 262
4. N Tuteja R Tuteja DNA helicases: the long unwinding road Nat Genet 13 1996 11 12
5. EP Benditt JM Benditt Evidence for a monoclonal origin of human atherosclerotic plaques Proc Natl Acad Sci USA 70 1973 1753 1756