OBEZİTENİN NADİR BİR NEDENİ: BARDET BİEDLE SENDROMU

Autor: İhsan Üstün, Mustafa Arı, Cumali Gökçe, Vefik Arıca, Mesut Coşkun, Murat Çelik, Kamil Cezgin, Burak Akçay

Publikováno v: Volume: 1, Issue: 1 47-49
The Medical Journal of Mustafa Kemal University
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 1, Iss 1, Pp 47-49 (2015)

Bardet Biedle Syndrome is a pleiotropic disorder with variable expressivity. Up to date fourteen BBS gene mutations have been reported. Primary cilia are microtubule-based membrane projections located at the surface of many cells and defects in prima

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ec89993ce80569ff83889b99ed450415
https://hdl.handle.net/20.500.12483/439