Leber's hereditary optic neuropathy : the clinical relevance of different mitochondrial DNA mutations
- Author
- RIORDAN-EVA, P1 ; HARDING, A. E
[1] National hosp. neurology neurosurgery, dep. neuro-ophthalmology, London WC1N 3BG, United Kingdom - Conference title
- British medical genetics conference
- Conference name
- British medical genetics conference (York 1994-09-12)
- Author (monograph)
- Clinical Genetics Society (Funder/Sponsor)
Clinical Molecular Genetics Society (Funder/Sponsor)
Genetical Society (Funder/Sponsor)
Genetic Nurses and Social Workers Association (Funder/Sponsor) - Source
Journal of medical genetics. 1995, Vol 32, Num 2, pp 81-87 ; ref : 71 ref
- Publisher
- BMJ, London
- Publication country
- United Kingdom
- Document type
- Conference Paper
- Language
- English
- Keyword (fr)
- Dégénérescence neurorétinienne héréditaire Leber Homme Mutation Maladie héréditaire Oeil pathologie Rétinopathie
- Keyword (en)
- Leber amaurosis Human Mutation Genetic disease Eye disease Retinopathy
- Keyword (es)
- Degeneración neuroretiniana hereditaria Leber Hombre Mutación 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
- 3418601
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
10.1136/jmg.32.2.81 
https://dx.doi.org/10.1136/jmg.32.2.81
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