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Latest Publications and Research on ADA2 Protein Deficiency

Clin. Exp. Rheumatol.      

Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation.

van Well GTJ, Kant B, van Nistelrooij A, Sirma Ekmekci S, Henriet SV, Hoppenreijs E, van Deuren M, van Montfrans J, Nierkens S, Gül A, van Gijn ME

To describe phenotypic and functional characteristics of patients with the homozygous c.973-2A>G splice site mutation in the adenosine deaminase 2 (AD ... Read More

Source: PubMed

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