A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date - Concepedia

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A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date

DOI Full Paper Access

56

Citations

21

References

2010

Year

Celia L. Gregson, P. Hollingworth, K A Petrie, Alex N. Bullock, Matthew A. Brown, Jonathan H. Tobias, James T. Triffitt

FibrosisProgressiva VariantPathologyBenign CaseNovel Acvr1 MutationMedicineCell BiologyExtracellular MatrixConnective Tissue Disease

References

	Year	Citations

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