High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection
- Author
- COLLER, Hilary A1 ; KHRAPKO, Konstantin2 ; BODYAK, Natalya D2 ; NEKHAEVA, Ekaterina2 ; HERRERO-JIMENEZ, Pablo3 ; THILLY, William G3
[1] Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98119, United States
[2] Beth Deaconess Israel Medical Center and Harvard, Medical School, Boston, Massachusetts 02115, United States
[3] Center for Environmental Health Sciences, Division of Bioengineering and Environmental Health, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States - Source
Nature genetics. 2001, Vol 28, Num 2, pp 147-150 ; ref : 25 ref
- Publisher
- Nature Publishing Group, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- DNA mitochondrial Homme Mutation Homoplasmie Tumeur
- Keyword (en)
- Mitochondrial DNA Human Mutation Tumor
- Keyword (es)
- DNA mitocondrial Hombre Mutación Tumor
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution / 002A07C Classical genetics, quantitative genetics, hybrids / 002A07C03 Human
- Discipline
- Eukaryotes genetics. Biological and molecular evolution
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1057212
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1038/88859 
https://dx.doi.org/10.1038/88859
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