For citation: Valieva S.I., Kurbanova S.Kh., Sologub A.S., Gaziev I.R., Ovsyannikov D.Yu. Diagnostic challenges in Blau syndrome: case report of pediatric patient with confirmed NOD2 gene mutation. Clinical review for general practice. 2025; 6 (11): 27–33 (In Russ.). DOI: 10.47407/kr2025.6.11.00707
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