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bn:03438050n

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JA

LEOPARD症候群

EN

Noonan syndrome with multiple lentigines which is part of a group called Ras/MAPK pathway syndromes, is a rare autosomal dominant, multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene. Wikipedia

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リウマチ学

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JA

LEOPARD症候群