A novel mutation of the WRN gene in a Chinese patient with Werner syndrome
- Author
- ZHAO, N1 ; HAO, F1 2 ; QU, T2 ; ZUO, Y.-G1 2 ; WANG, B-X2
[1] Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking, China
[2] Department of Dermatology, Southwest Hospital, Chongqing, China - Source
Clinical and experimental dermatology (Print). 2008, Vol 33, Num 3, pp 278-281, 4 p ; ref : 7 ref
- CODEN
- CEDEDE
- ISSN
- 0307-6938
- Scientific domain
- Dermatology
- Publisher
- Blackwell, London
/
Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Chinois Dermatologie Gène Homme Mutation Syndrome de Werner Chine Maladie héréditaire Pathologie de l'oeil Pathologie de la peau Asie
- Keyword (en)
- Chinese Dermatology Gene Human Mutation Werner syndrome China Genetic disease Eye disease Skin disease Asia
- Keyword (es)
- Chino Dermatología Gen Hombre Mutación Werner síndrome China Enfermedad hereditaria Ojo patología Piel patología Asia
- Classification
- Discipline
- Dermatology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20272776
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
10.1111/j.1365-2230.2007.02641.x 
https://dx.doi.org/10.1111/j.1365-2230.2007.02641.x
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