Associated Papers
Structural Basis of the Human Endoglin-BMP9 Interaction: Insights into BMP Signaling and HHT1.
Saito T et al.
Cell Reports, 2017
Functional analysis of endoglin mutations from hereditary hemorrhagic telangiectasia type 1 patients reveals different mechanisms for endoglin loss of function.
Mallet C et al.
Human Molecular Genetics, 2015
A case of delayed-onset hereditary hemorrhagic telangiectasia with a frameshift ENG mutation.
Akagawa H et al.
Neurology India, 0
Autologous correction in patient induced pluripotent stem cell-endothelial cells to identify a novel pathogenic mutation of hereditary hemorrhagic telangiectasia.
Zhou F et al.
Pulmonary Circulation, 0
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