Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Liskova P; Ulmanova O; Tesina P; Melsova H; Diblik P; Hansikova H; Tesarova M; Votruba M; Acta Ophthalmologica, 2013, vol. 91, issue 3, p e225, ISSN 17553768. ISBN 17553768.

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