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  1. 1.Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder

    Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder  / Liskova P., Ulmanova O. ... [et al.] .  Acta ophthalmologica . - Vol. 91, no. 3 (2013), s. e225-e231   [Dokument nie je vo fonde knižnice]
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