000 01450 a2200433 4500
005 20250515230340.0
264 0 _c20101021
008 201010s 0 0 eng d
022 _a1744-5094
024 7 _a10.3109/13816810.2010.492818
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVillanueva-Mendoza, Cristina
245 0 0 _aFamilial case of Blau syndrome associated with a CARD15/NOD2 mutation.
_h[electronic resource]
260 _bOphthalmic genetics
_cSep 2010
300 _a155-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aArthritis, Rheumatoid
_xgenetics
650 0 4 _aExanthema
_xgenetics
650 0 4 _aFemale
650 0 4 _aFluorescein Angiography
650 0 4 _aHumans
650 0 4 _aJoint Diseases
_xgenetics
650 0 4 _aNod2 Signaling Adaptor Protein
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPoint Mutation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aRecurrence
650 0 4 _aSyndrome
650 0 4 _aUveitis, Anterior
_xgenetics
650 0 4 _aYoung Adult
700 1 _aArellanes-García, Lourdes
700 1 _aCubas-Lorenzo, Victoria
700 1 _aJimenez-Martinez, Maria C
700 1 _aFlores-Suárez, Luis Felipe
700 1 _aZenteno, Juan Carlos
773 0 _tOphthalmic genetics
_gvol. 31
_gno. 3
_gp. 155-8
856 4 0 _uhttps://doi.org/10.3109/13816810.2010.492818
_zAvailable from publisher's website
999 _c19913916
_d19913916