Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability

Autor: Gyri Aasland Gradek, Olaug K. Rødningen, Bjørn Ivar Haukanes, Atle Brendehaug, Gunnar Helland, Gunnar Houge, Siren Berland, Ernie M.H.F. Bongers, Rolph Pfundt, Nicole de Leeuw, Randi Hovland, Stefan Johansson, Madeleine Fannemel

Publikováno v: American Journal of Medical Genetics. Part A, 164, 7, pp. 1622-6
American Journal of Medical Genetics. Part A, 164, 1622-6

Item does not contain fulltext MEIS2 is a homeodomain-containing transcription factor of the TALE superfamily that has been proven important for development. We confirm and extend a recent single clinical report stating that deletions in MEIS2 can ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdf855f5eff49f9555f5ed17329323a3
https://hdl.handle.net/2066/138141