A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2022

Altmetric Badge

Mentioned by

So far, Dimensions has found 2 publications that cite this research output.

Article in 中华医学遗传学杂志 (October 2023)

Article in Molecular and Cellular Biochemistry (April 2023)

This page shows the most recent citations of this research output.

Click here to find out how to access more activity.