No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
about
Complex and multi-allelic copy number variation in human diseaseCopy number variation of FCGR genes in etiopathogenesis of sarcoidosisFcγ receptors: genetic variation, function, and disease.Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method.Reply to 'comment on no association of primary Sjögren's syndrome with Fcγ receptor gene variants'.
P2860
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
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2013 nî lūn-bûn
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No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@en
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@nl
type
label
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@en
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@nl
prefLabel
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@en
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@nl
P2093
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P50
P356
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P1476
No association of primary Sjögren's syndrome with Fcγ receptor gene variants.
@en
P2093
A I Bolstad
C P D Fernandes
E Theander
G Kristjansdottir
G Nordmark
K Haldorsen
L Rönnblom
M Kvarnström
P2860
P2888
P304
P356
10.1038/GENE.2013.12
P577
2013-04-04T00:00:00Z