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

M. Kirschner, A. -S. Bouillon, Ventura M. Ferreira,A. Maurer, S. Wilop, F. Thol,A. Roeth,U. Platzbecker,W. Blau, F. A. Ayuk, S. Corbacioglu, H. Schrezenmeier, M. Manz, L. Ebel,S. Koschmieder,M. Schemionek,S. Isfort,J. Panse, T. H. Brmmendorf,F. Beier

Onkologie(2017)

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