OALib Journal期刊
ISSN: 2333-9721
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Autosomal dominant optic atrophy and cataract “plus” phenotype including axonal neuropathy
DOI: 10.1212/NXG.0000000000000322
Adriana P. Rebelo, Alan M. Pittman, Alejandro Horga, Andrea Cortese, Andreea Manole, Catherine E. Woodward, Enrico Bugiardini, Fion Bremner, Henry Houlden, Iain P. Hargreaves, James M. Polke, Lois Dankwa, Mary M. Reilly, Michael G. Hanna, Robert D.S. Pitceathly, Sebastian Brandner, Stephan Züchner, Steven S. Scherer, Zane Jaunmuktane
Abstract:
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