Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms
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,Volume:
10
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-015-0248-3
Date:
December, 2015
File:
PDF, 1.12 MB
english, 2015