P75 Infantile reversible COX deficiency myopathy caused by the m.14674T>C mutation in mt-tRNAGlu in a German family

✍ Scribed by R. Horvath; J.P. Kemp; H.A.L. Tuppen; G. Hudson; A. Pyle; E. Holinski-Feder; A. Abicht; B. Czermin; M.C. Walter; A. Günther-Scholz; P.M. Smith; R. McFarland; Z.M.A. Chrzanowska-Lightowlers; R.N. Lightowlers; H. Lochmüller; R.W. Taylor; P.F. Chinnery

• Book ID: 117670239
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 48 KB
• Volume: 20
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/s0960-8966(10)70090-0