A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function. (Q47911970)

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scientific article published in January 2017
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A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.
scientific article published in January 2017

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    A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function (English)

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