A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

✍ Scribed by Levesque, Sebastien (author);Morin, Charles (author);Guay, Simon Pierre (author);Villeneuve, Josee (author);Marquis, Pascale (author);Yik, Wing Y. (author);Jiralerspong, Sarn (author);Bouchard, Luigi (author);Steinberg, Steven (author);Hacia, Joseph G. (author);Dewar, Ken (author);Braverman, Nancy E. (author)

• Book ID: 119896658
• Publisher: BioMed Central
• Year: 2012
• Tongue: English
• Weight: 696 KB
• Volume: 13
• Category: Article
• ISSN: 1471-2350
• DOI: 10.1186/1471-2350-13-72