A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa
- Author
- FARRAR, G. J; KENNA, P; JORDAN, S. A; KUMAR-SINGH, R; HUMPHRIES, M. M; SHARP, E. M; SHEILS, D. M; HUMPHRIES, P
Trinity coll. Dublin, dep. genetics, Dublin, Ireland - Source
Nature (London). 1991, Vol 354, Num 6353, pp 478-480 ; ref : 28 ref
- CODEN
- NATUAS
- ISSN
- 0028-0836
- Scientific domain
- Multidisciplinary
- Publisher
- Nature Publishing, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Délétion Etude familiale Homme Rétinite pigmentaire Gène RDS Périphérine Glycoprotéine Maladie héréditaire Oeil pathologie Rétinopathie
- Keyword (en)
- Deletion Family study Human Retinitis pigmentosa Glycoproteins Genetic disease Eye disease Retinopathy
- Keyword (es)
- Deleción Estudio familiar Hombre Retinitis pigmentaria Glicoproteina Enfermedad hereditaria Ojo patología Retinopatía
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B09 Ophthalmology / 002B09I Retinopathies
- Discipline
- Ophthalmology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5147275
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
10.1038/354478a0 
https://dx.doi.org/10.1038/354478a0
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