Blau syndrome is an inherited granulomatous disease caused by gain-of-function mutations in the NOD2 gene.
El síndrome de Blau es una enfermedad granulomatosa hereditaria causada por mutaciones de ganancia de función en el gen NOD2.
Front | An inherited granulomatous disease caused by gain-of-function mutations in the, NOD2, gene |
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Back | Blau syndrome |
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