We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMissense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.AuthorsBeysen, Diane; Moumné, Lara; Veitia, Reiner; Peters, Hartmut; Leroy, Bart P.; De Paepe, Anne; De Baere, ElfridePublicationHuman Molecular Genetics, 2008, Vol 17, Issue 13, p2030ISSN0964-6906Publication typearticleDOI10.1093/hmg/ddn100