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16. Les auteurs

27. A plasma metabolomic signature of Leber hereditary optic neuropathy showing taurine and nicotinamide deficiencies

30. Mapping of a congenital microcoria locus to 13q31-q32

35. Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome

36. Cas cliniques en ophtalmologie

39. Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations

40. Preservation of automatic ocular saccades in healthy elderly: alteration in patients with dementia with Lewy body

41. Auteurs et collaborateurs

48. Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy

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