Heterozygous RTEL1 variants are associated with bone marrow failure in cryptic dyskeratosis congenita - first results from the Aachen telomere registry

Kirschner, M. and Bouillon, A. -S. and Ferreira, Ventura M. and Maurer, A. and Wilop, S. and Thol, F. and Roeth, A. and Platzbecker, U. and Blau, W. and Ayuk, F. A. and Corbacioglu, S. and Schrezenmeier, H. and Manz, M. and Ebel, L. and Koschmieder, S. and Schemionek, M. and Isfort, S. and Panse, J. and Brmmendorf, T. H. and Beier, F. (2017) Heterozygous RTEL1 variants are associated with bone marrow failure in cryptic dyskeratosis congenita - first results from the Aachen telomere registry. ONCOLOGY RESEARCH AND TREATMENT, 40 (Suppl3). p. 252. ISSN 2296-5270, 2296-5262

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Item Type:	Article
Subjects:	600 Technology > 610 Medical sciences Medicine
Divisions:	Medicine > Abteilung für Pädiatrische Hämatologie, Onkologie und Stammzelltransplantation
Depositing User:	Petra Gürster
Date Deposited:	14 Dec 2018 13:15
Last Modified:	17 Sep 2020 06:17
URI:	https://pred.uni-regensburg.de/id/eprint/1270

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