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Fibrodysplasia ossificans progressiva / ACVR1 / BMPR2 / Signal transduction / Microsatellite / Mutation / Activin and inhibin / Biology / Genetics / International FOP Association


B R I E F C O M M U N I C AT I O N S A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia
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Document Date: 2008-04-22 09:31:57


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File Size: 198,29 KB

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