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Search Results - van Nistelrooij, Annabel
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Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation
by
van Well, Gijs T J
,
Kant, Benjamin
,
van Nistelrooij, Annabel
,
Sirma Ekmekci, Sema
,
Henriet, Stefanie V
,
Hoppenreijs, Esther
,
van Deuren, Marcel
,
van Montfrans, Joris
,
Nierkens, Stefan
,
Gül, Ahmet
,
van Gijn, Mariëlle E
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Clinical and experimental rheumatology
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Clinical And Experimental Rheumatology
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Adenosine Deaminase - Deficiency
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Adenosine Deaminase - Genetics
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Behcet Syndrome - Genetics
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Biological Variation, Population
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Genetic Association Studies
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Homozygote
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Humans
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Intercellular Signaling Peptides And Proteins - Deficiency
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Intercellular Signaling Peptides And Proteins - Genetics
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Mutation - Genetics
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Freely Accessible Science Journals - Check A-Z Of Ejournals
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