000 01348 a2200373 4500
005 20250515191439.0
264 0 _c20091217
008 200912s 0 0 eng d
022 _a1875-8630
024 7 _a10.3233/DMA-2009-0639
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRodríguez-Pérez, Noelia
245 0 0 _aBlau syndrome-related CARD15/NOD2 mutations are not linked to idiopathic uveitis in Spanish patients.
_h[electronic resource]
260 _bDisease markers
_c2009
300 _a1-5 p.
_bdigital
500 _aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCase-Control Studies
650 0 4 _aDNA
_xblood
650 0 4 _aHumans
650 0 4 _aMutation
_xgenetics
650 0 4 _aNod2 Signaling Adaptor Protein
_xgenetics
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aSpain
650 0 4 _aSyndrome
650 0 4 _aUveitis
_xblood
700 1 _aAguinaga-Barrilero, Ana
700 1 _aGorroño-Echebarría, Marina B
700 1 _aPérez-Blas, Mercedes
700 1 _aMartín-Villa, José M
773 0 _tDisease markers
_gvol. 27
_gno. 1
_gp. 1-5
856 4 0 _uhttps://doi.org/10.3233/DMA-2009-0639
_zAvailable from publisher's website
999 _c19216558
_d19216558