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pro vyhledávání: '"Birgit Groff-Kellermann"'
Autor:
George M. Martin, Norberto López, Kivanc Cefle, Davor Lessel, Sukru Ozturk, Junko Oshima, Joerg Schmidtke, P. F. Ippel, Bhaskar Saha, Gudrun Nürnberg, Joseph Boak, Fuki M. Hisama, Dru F. Leistritz, Daniel Eyman, Martin Poot, Katrin Friedrich, Holger Hoehn, Dincy Peter, María J. Garcia-F-Villalta, Lin Lee, Theda Wessel, Carolien M. Kets, Peter Nürnberg, Peter C. van den Akker, Christian Kubisch, Vítor Tedim Cruz, Birgit Groff-Kellermann, Chumei Li, Goli Compoginis
Publikováno v:
Human Genetics, 128, 103-11
HUMAN GENETICS, 128(1), 103-111. SPRINGER
Human Genetics, 128, 1, pp. 103-11
HUMAN GENETICS, 128(1), 103-111. SPRINGER
Human Genetics, 128, 1, pp. 103-11
Item does not contain fulltext Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations at the WRN locus, which codes for a member of the RecQ family of DNA helicases. Since 1988, the International Registry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b70c3168e5331a43b20253ab0c5c8f
https://doi.org/10.1007/s00439-010-0832-5
https://doi.org/10.1007/s00439-010-0832-5
