Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms
一名男性患有脂肪酸酰胺水解酶 2 缺陷，并出现神经和精神症状
期刊:Orphanet Journal of Rare Diseases
影响因子:3.4
doi:10.1186/s13023-015-0248-3
Sandra Sirrs, Clara D M van Karnebeek, Xiaoxue Peng, Casper Shyr, Maja Tarailo-Graovac, Rupasri Mandal, Daniel Testa, Devin Dubin, Gregory Carbonetti, Steven E Glynn, Bryan Sayson, Wendy P Robinson, Beomsoo Han, David Wishart, Colin J Ross, Wyeth W Wasserman, Trevor A Hurwitz, Graham Sinclair, Marti
