Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient

✍ Scribed by Alberto Blázquez; Mari Carmen Gil-Borlado; María Morán; Alfonso Verdú; María Rosario Cazorla-Calleja; Miguel A. Martín; Joaquín Arenas; Cristina Ugalde

• Book ID: 116793852
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 225 KB
• Volume: 19
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2008.11.016