An atypical Leber's hereditary optic neuropathy with the 11778 mutation.
Identifieur interne : 000872 ( Istex/Corpus ); précédent : 000871; suivant : 000873An atypical Leber's hereditary optic neuropathy with the 11778 mutation.
Auteurs : Y. Hotta ; M. Hayakawa ; K. Fujiki ; K. Shinohara ; K. Sado ; A. Kanai ; K. YanashimaSource :
- British Journal of Ophthalmology [ 0007-1161 ] ; 1993-11.
English descriptors
- Teeft :
- Acuity, Double vision, Fujiki, Hayakawa, Hotta, Human lymphotropic virus type, Human retrovirology, Immunogenetic factors, John radcliffe hospital, Leucocyte, Lhon, Lott, Minor colour disturbance, Mitochondrial, Mochizuki, Mtdna, Mtdna pattern, Mutant, Mutant mtdna, Mutation, Mycoplasma, Neuropathy, Ophthalmic clinic, Ophthalmol, Ophthalmology, Optic, Optic neuropathy, Pathogenesis, Pathological processes, Pneumoniae, Polymerase, Polymerase chain reaction, Raven press, Remarkable change, Respiratory tract, Tract infection, Uveitis, Visual acuities, Visual acuity, Watanabe, Yamaguchi, Yoshimura.
Url:
DOI: 10.1136/bjo.77.11.748
Links to Exploration step
ISTEX:A22364824C700020104F690975EBBF859C7DDA8BLe document en format XML
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