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6. Familial Blau syndrome without uveitis caused by a novel mutation in the nucleotide-binding oligomerization domain-containing protein 2 gene with good response to infliximab. Toral-López J; González-Huerta LM; Martín-Del Campo M; Messina-Baas O; Cuevas-Covarrubias SA Pediatr Dermatol; 2018 May; 35(3):e180-e183. PubMed ID: 29570830 [TBL] [Abstract][Full Text] [Related]
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17. Blau syndrome with pulmonary nodule in a child. Su J; Liu D Australas J Dermatol; 2021 May; 62(2):217-220. PubMed ID: 33742458 [TBL] [Abstract][Full Text] [Related]
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