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. LaforêtVolume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.1067
File:
PDF, 48 KB
english, 2011