000 01470 a2200409 4500
005 20250516233459.0
264 0 _c20160106
008 201601s 0 0 eng d
022 _a1476-5438
024 7 _a10.1038/ejhg.2014.158
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBakir-Gungor, Burcu
245 0 0 _aIdentification of possible pathogenic pathways in Behçet's disease using genome-wide association study data from two different populations.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_cMay 2015
300 _a678-87 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBehcet Syndrome
_xdiagnosis
650 0 4 _aComputational Biology
_xmethods
650 0 4 _aDatabases, Genetic
650 0 4 _aDatasets as Topic
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenome-Wide Association Study
650 0 4 _aHumans
650 0 4 _aJapan
650 0 4 _aPhenotype
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aSignal Transduction
650 0 4 _aTurkey
700 1 _aRemmers, Elaine F
700 1 _aMeguro, Akira
700 1 _aMizuki, Nobuhisa
700 1 _aKastner, Daniel L
700 1 _aGul, Ahmet
700 1 _aSezerman, Osman U
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 23
_gno. 5
_gp. 678-87
856 4 0 _uhttps://doi.org/10.1038/ejhg.2014.158
_zAvailable from publisher's website
999 _c24196182
_d24196182