Identification of a novel compound heterozygote SCO2 mutation in cytochrome c oxidase deficient fatal infantile cardioencephalomyopathy

✍ Scribed by M Knuf; J Faber; R G Huth; P Freisinger; F Zepp; C Kampmann

• Book ID: 114814915
• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 127 KB
• Volume: 96
• Category: Article
• ISSN: 0803-5253
• DOI: 10.1111/j.1651-2227.2007.00008.x