Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome families
- Autor
- DOMENECH, E1 ; GOMEZ-ZAERA, M1 ; NUNES, V1
[1] Centre de Genètica Mèdica i Molecular, Institut de Recerca Oncològica (I.R.O.), L'Hospitalet de Llobregat, Barcelona, Spain - Fuente
Clinical genetics. 2004, Vol 65, Num 6, pp 463-469, 7 p ; ref : 30 ref
- Editor
- Blackwell, Oxford
- País de la publicación
- United Kingdom
- Tipo de documento
- Article
- Idioma
- English
- Palabra clave de autor
- DIDMOAD WFS1 gene Wolfram syndrome mtDNA rearrangements mutations
- Palabra clave (fr)
- DNA mitochondrial Espagnol Etude familiale Gène Mutation Wolfram syndrome Maladie héréditaire Syndrome complexe
- Palabra clave (in)
- Mitochondrial DNA Spanish Family study Gene Mutation Wolfram syndrome Genetic disease Complex syndrome
- Palabra clave (es)
- DNA mitocondrial Español Estudio familiar Gen Mutación Wolfram síndrome Enfermedad hereditaria Síndrome complejo
- Clasificación
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23E Complex syndromes
- Disciplina
- Medical genetics
- Procedencia
- Inist-CNRS
- Base de datos
- PASCAL
- Identificador INIST
- 15749174
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.1399-0004.2004.00249.x 
https://dx.doi.org/10.1111/j.1399-0004.2004.00249.x
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