Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms
- Author
- SITTLER, A; DEVYS, D; WEBER, C; MANDEL, J.-L
CNRS INSERM ULP, inst. génétique biologie moléculaire cellulaire, 67604 Illkirch, France - Source
Human molecular genetics (Print). 1996, Vol 5, Num 1, pp 95-102 ; ref : 34 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Biologie moléculaire Epissage alternatif Expression génique Forme moléculaire Gène Homme Localisation Produit gène Protéine X fragile syndrome Fragilité chromosomique
- Keyword (en)
- Molecular biology Alternative splicing Gene expression Molecular form Gene Human Localization Gene product Proteins Fragile X syndrome Chromosome fragility
- Keyword (es)
- Biología molecular Empalme alternativo Expresión genética Forma molecular Gen Hombre Localización Producto gene Proteína X frágil síndrome Fragilidad cromosómica
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23C Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2957180
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
10.1093/hmg/5.1.95 
https://dx.doi.org/10.1093/hmg/5.1.95
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