Wikidata

(Q40205916)

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

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title
Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17553686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17553686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 December 2019
author name string

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