Biallelic mutations in M1AP are associated with meiotic arrest, severely impaired spermatogenesis and male infertility

Friedrich, C.Nagirnaja, L.Oud, M. S.Lopes, A. M.van der Heijden, G. W.Heald, J.Rotte, N.Wistuba, J.Woeste, M.Ledig, S.Krenz, H.Smits, R. M.Carvalho, F.Goncalves, J.Fietz, D.Turkgenc, B.Ergoren, M. C.Cetinkaya, M.Basar, M.Kahraman, S.McEleny, K.Xavier, M. J.Turner, H.Pilatz, A.Roepke, A.Dugas, M.Kliesch, S.Neuhaus, N.Aston, K. I.Conrad, D. F.Veltman, J. A.Wyrwoll, M. J.Tuettelmann, F.2024-07-032024-07-032020-12-011018-4813https://hdl.handle.net/11452/42774eninfo:eu-repo/semantics/closedAccessScience & technologyLife sciences & biomedicineBiochemistry & molecular biologyGenetics & heredityBiochemistry & molecular biologyGenetics & heredityBiallelic mutations in M1AP are associated with meiotic arrest, severely impaired spermatogenesis and male infertilityMeeting Abstract0005984826034291002100328SUPPL 1, Supplement 1