Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes.
(Q40205916)
scientific article published on 6 May 2007
scientific article published on 6 May 2007
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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 |
External Links
| (P356) |
10.1016/J.NBD.2007.04.012
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| (P698) |
17553686
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