Functional comparison of human ACVR1 and zebrafish Acvr1l FOP‐associated variants in embryonic zebrafish
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DOI: 10.1002/dvdy.566
Abstract: Fibrodysplasia ossificans progressiva (FOP), a rare disease characterized by progressive heterotopic ossification of muscle and connective tissues, is caused by autosomal dominant activating mutations in the type I receptor, ACVR1/ALK2. The classic human FOP variant,… read more here.
Keywords: comparison human; zebrafish; fop; human acvr1 ... See more keywords