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

Journal

BMC Neurology

Journal Volume

17

Journal Issue

1

Pages

2

Date Issued

2017

Author(s)

Hsueh S.-J.

Lin H.-I.

DOI

10.1186/s12883-016-0781-2

URI

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010223530&doi=10.1186%2fs12883-016-0781-2&partnerID=40&md5=45cf33e1065609eed4ab764c7f8ed9d3

https://scholars.lib.ntu.edu.tw/handle/123456789/507552

SDGs

[SDGs]SDG3

Publisher

BioMed Central Ltd.

Type

journal article