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

✍ Scribed by G.F. Polara; A. Behin; T. Stojkovic; M. Gilleron; C. Jardel; K. Wahbi; B. Eymard; P. Laforêt

• Book ID: 116794880
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 48 KB
• Volume: 21
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2011.06.1067