Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms-Reference-Cited by-同舟云学术

Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms

Published:2015-03-28 Issue:1 Volume:10 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Sirrs Sandra,van Karnebeek Clara DM,Peng Xiaoxue,Shyr Casper,Tarailo-Graovac Maja,Mandal Rupasri,Testa Daniel,Dubin Devin,Carbonetti Gregory,Glynn Steven E,Sayson Bryan,Robinson Wendy P,Han Beomsoo,Wishart David,Ross Colin J,Wasserman Wyeth W,Hurwitz Trevor A,Sinclair Graham,Kaczocha Martin

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-015-0248-3.pdf

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3. Battisa N, Bari M, Tarditi A, Mariotti C, Bachoud-Lévi AC, Zuccato C, et al. Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington’s disease mutation in peripheral lymphocytes. Neurobiol Dis. 2007;27:108–16.

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