Publication: Biallelic mutations in M1AP are associated with meiotic arrest, severely impaired spermatogenesis and male infertility
dc.contributor.author | Friedrich, C. | |
dc.contributor.author | Nagirnaja, L. | |
dc.contributor.author | Oud, M. S. | |
dc.contributor.author | Lopes, A. M. | |
dc.contributor.author | van der Heijden, G. W. | |
dc.contributor.author | Heald, J. | |
dc.contributor.author | Rotte, N. | |
dc.contributor.author | Wistuba, J. | |
dc.contributor.author | Woeste, M. | |
dc.contributor.author | Ledig, S. | |
dc.contributor.author | Krenz, H. | |
dc.contributor.author | Smits, R. M. | |
dc.contributor.author | Carvalho, F. | |
dc.contributor.author | Goncalves, J. | |
dc.contributor.author | Fietz, D. | |
dc.contributor.author | Turkgenc, B. | |
dc.contributor.author | Ergoren, M. C. | |
dc.contributor.author | Cetinkaya, M. | |
dc.contributor.author | Basar, M. | |
dc.contributor.author | Kahraman, S. | |
dc.contributor.author | McEleny, K. | |
dc.contributor.author | Xavier, M. J. | |
dc.contributor.author | Turner, H. | |
dc.contributor.author | Pilatz, A. | |
dc.contributor.author | Roepke, A. | |
dc.contributor.author | Dugas, M. | |
dc.contributor.author | Kliesch, S. | |
dc.contributor.author | Neuhaus, N. | |
dc.contributor.author | Aston, K. I. | |
dc.contributor.author | Conrad, D. F. | |
dc.contributor.author | Veltman, J. A. | |
dc.contributor.author | Wyrwoll, M. J. | |
dc.contributor.author | Tuettelmann, F. | |
dc.contributor.buuauthor | TEMEL, ŞEHİME GÜLSÜN | |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Genetik Anabilim Dalı. | |
dc.contributor.researcherid | AAG-8385-2021 | |
dc.date.accessioned | 2024-07-03T07:23:28Z | |
dc.date.available | 2024-07-03T07:23:28Z | |
dc.date.issued | 2020-12-01 | |
dc.description.sponsorship | DFG Clinical Research Unit "Male Germ Cells: from Genes to Function" CRU326 | |
dc.identifier.endpage | 1003 | |
dc.identifier.issn | 1018-4813 | |
dc.identifier.issue | SUPPL 1, Supplement 1 | |
dc.identifier.startpage | 1002 | |
dc.identifier.uri | https://hdl.handle.net/11452/42774 | |
dc.identifier.volume | 28 | |
dc.identifier.wos | 000598482603429 | |
dc.indexed.wos | WOS.SCI | |
dc.language.iso | en | |
dc.publisher | Springernature | |
dc.relation.journal | European Journal Of Human Genetics | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Science & technology | |
dc.subject | Life sciences & biomedicine | |
dc.subject | Biochemistry & molecular biology | |
dc.subject | Genetics & heredity | |
dc.subject | Biochemistry & molecular biology | |
dc.subject | Genetics & heredity | |
dc.title | Biallelic mutations in M1AP are associated with meiotic arrest, severely impaired spermatogenesis and male infertility | |
dc.type | Meeting Abstract | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | f513efaa-a54e-4cfa-840f-28e2fbdc001a | |
relation.isAuthorOfPublication.latestForDiscovery | f513efaa-a54e-4cfa-840f-28e2fbdc001a |