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Clinical phenotype and CARD15 gene mutation with Blau Syndrome in Chinese children and their parents

2008-01-01

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Literature Corpus work: 7428c713-2d9c-5d0e-8aeb-62c0cd1e4e08
DOI: 10.1186/1546-0096-6-s1-p210
PMCID: PMC3334015

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