Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes

✍ Scribed by Natalia Battista; Monica Bari; Alessia Tarditi; Caterina Mariotti; Anne-Catherine Bachoud-Lévi; Chiara Zuccato; Alessandro Finazzi-Agrò; Silvia Genitrini; Marc Peschanski; Stefano Di Donato; Elena Cattaneo; Mauro Maccarrone

• Book ID: 113812152
• Publisher: Elsevier Science
• Year: 2007
• Tongue: English
• Weight: 645 KB
• Volume: 27
• Category: Article
• ISSN: 0969-9961
• DOI: 10.1016/j.nbd.2007.04.012