Fingerprint
Dive into the research topics of 'A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands
Meropi Toumba, Vassos Neocleous, Christos Shammas, Violetta Anastasiadou, Jeremy Allgrove, Leonidas A. Phylactou, Nicos Skordis
Research output: Contribution to journal › Article › peer-review
2
Citations
(Scopus)