Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes. (Q40205916)
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scientific article published on 6 May 2007
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes. |
scientific article published on 6 May 2007 |
Statements
Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes (English)
Monica Bari
Alessia Tarditi
Caterina Mariotti
Alessandro Finazzi-Agrò
Silvia Genitrini
Stefano Di Donato
Mauro Maccarrone