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, Wendy P; Han, Beomsoo; Wishart, David; Ross, Colin J; Wasserman, Wyeth W; Hurwitz, Trevor A; Sinclair, Graham; Kaczocha, Martin

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

Naziv:	Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms
Autori:	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;
Godina:	2015
Publikacija:	Orphanet Journal of Rare Diseases
ISSN:	1750-1172 Orphanet Journal of Rare Diseases Pretraži identifikator
Tip rezultata:	Naučni članak
Kolacija:	vol. 10 br. 1
DOI:	10.1186/s13023-015-0248-3
WoS-ID:	000354015400001
Scopus-ID:	2-s2.0-84928894998
PMID:	25885783
PMCID:	PMC4423390
URI:	https://enauka.gov.rs/handle/123456789/247369
Izvor metapodataka:	Migrirano iz RIS podataka
M-kategorija:	21M21 - Rad u vrhunskom međ. časopisu

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