Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes.
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| Description | scientific article published on 6 May 2007 |
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author: Anne-Catherine Bachoud-Lévi Natalia Battista Chiara Zuccato Elena Cattaneo Marc Peschanski |
| Publication date | May 6, 2007 |
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