A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva - Concepedia

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A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

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Citations

12

References

2006

Year

Eileen M. Shore, Meiqi Xu, George Feldman, David Fenstermacher, Tae‐Joon Cho, In Ho Choi, J. M. Connor, Patricia Delai, David L. Glaser, Martine LeMerrer,

Nature Genetics

Recurrent MutationFibrosisSignal TransductionBmp TypeSporadic Fibrodysplasia OssificansBone Morphogenic ProteinGenetic DisorderPathogenesisPathologyOsteogenesisMedicineCell BiologyCell SignalingConnective Tissue Disease

References

	Year	Citations

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