P5.38 Clinical features of autosomal dominant...

P5.38 Clinical features of autosomal dominant ophthalmoplegia related to PEO1 gene mutations

G.F. Polara, A. Behin, T. Stojkovic, M. Gilleron, C. Jardel, K. Wahbi, B. Eymard, P. Laforêt
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Volume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.1067
File:
PDF, 48 KB
english, 2011
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