A rare hereditary connective tissue disease associated with the TGF-? signalling pathway:a case study of Loeys-Dietz syndrome type 1

Balasar, M.Oflaz, M. B.Emlik, G. D.2024-02-232024-02-2320191018-48131476-5438https://hdl.handle.net/20.500.12452/1733451st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY[Abstract Not Availabe]eninfo:eu-repo/semantics/closedAccess[Keyword Not Available]A rare hereditary connective tissue disease associated with the TGF-? signalling pathway:a case study of Loeys-Dietz syndrome type 1Conference Object27914914Q1WOS:000489313107095Q2