Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus

✍ Scribed by Soini, Heidi K. (author);Moilanen, Jukka S. (author);Vilmi-Kerälä, Tiina (author);Finnilä, Saara (author);Majamaa, Kari (author)

• Book ID: 120679331
• Publisher: BioMed Central
• Year: 2013
• Tongue: English
• Weight: 582 KB
• Volume: 14
• Category: Article
• ISSN: 1471-2350
• DOI: 10.1186/1471-2350-14-73