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pro vyhledávání: '"Ye-Oun Byeon"'
Autor:
Agnes Schröder, Talia Örs, Ye-Oun Byeon, Fabian Cieplik, Peter Proff, Christian Kirschneck, Eva Paddenberg
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 23, p 16581 (2023)
Cleidocranial dysplasia (CCD) is a rare genetic defect caused by a heterozygous mutation of runt-related transcription factor 2 (RUNX2), which is important for osteoblast and skeletal development. RUNX2-deficiency causes extra- and intra-oral malform
Externí odkaz:
https://doaj.org/article/21024959d45d42bb808614a52a5f1910
