Cite
HARVARD Citation
Ognenovski, M. et al. (2016). Whole Exome Sequencing Identifies Rare Protein‐Coding Variants in Behçet's Disease. Arthritis & rheumatology. 68 (5), pp. 1272-1280. [Online].
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Ognenovski, M. et al. (2016). Whole Exome Sequencing Identifies Rare Protein‐Coding Variants in Behçet's Disease. Arthritis & rheumatology. 68 (5), pp. 1272-1280. [Online].