A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review
Crossref DOI link: https://doi.org/10.1186/s12883-016-0781-2
Published Online: 2017-01-06
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Hsueh, Sung-Ju
Lee, Ni-Chung
Yang, Shu-Hua
Lin, Han-I
Lin, Chin-Hsien
Funding for this research was provided by:
Ministry of Science and Technology of Taiwan (MOST 104-2314-B-002-175-MY2)