A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review

Hsueh S.-J.NI-CHUNG LEESHU-HUA YANGLin H.-I.CHIN-HSIEN LIN2020-07-012020-07-0120171471-2377https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010223530&doi=10.1186%2fs12883-016-0781-2&partnerID=40&md5=45cf33e1065609eed4ab764c7f8ed9d3https://scholars.lib.ntu.edu.tw/handle/123456789/507552[SDGs]SDG3A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature reviewjournal article10.1186/s12883-016-0781-2280568722-s2.0-85010223530