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Published in 2018 at "Bone"
DOI: 10.1016/j.bone.2018.03.015
Abstract: Various substitution mutations in ALK2, a transmembrane serine/threonine kinase receptor for bone morphogenetic proteins (BMPs), have been identified in patients with genetic disorders such as fibrodysplasia ossificans progressiva (FOP), diffuse intrinsic pontine glioma (DIPG) and…
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Keywords:
signal transduction;
genetic disorders;
transduction alk2;
mutations associated ... See more keywords