Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I: Linkage analysis
- Author
- EIBERG, H1 ; KJER, B; KJER, P; ROSENBERG, T
[1] Univ. inst. medical biochemistry genetics, dep. medical genetics, 2200 Copenhagen, Denmark - Source
Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 977-980 ; ref : 22 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Atrophie Caractère dominant Carte génétique Chromosome A3 Homme Linkage Marqueur génétique Nerf optique Gène OPA1 Maladie héréditaire Nerf crânien pathologie Oeil pathologie Système nerveux pathologie
- Keyword (en)
- Atrophia Dominant character Genetic mapping A3-Chromosome Human Linkage Genetic marker Optic nerve Genetic disease Disorders of cranial nerves Eye disease Nervous system diseases
- Keyword (es)
- Atrofia Carácter dominante Mapa genético Cromosoma A3 Hombre Ligamiento Marcador genético Nervio óptico Enfermedad hereditaria Nervio craneal patología Ojo patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B09 Ophthalmology / 002B09L Diseases of visual field, optic nerve, optic chiasma and optic tracts
- Discipline
- Ophthalmology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4126375
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/3.6.977 
https://dx.doi.org/10.1093/hmg/3.6.977
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