Dyskeratosis congenita bei einem 40-jährigen Patienten
Author:
Publisher
Springer Science and Business Media LLC
Subject
Dermatology
Link
http://link.springer.com/content/pdf/10.1007/s00105-005-0937-2.pdf
Reference8 articles.
1. Alter BP, Gardner FH, Hall RE (1997) Treatment of dyskeratosis congenita with granulocyte colony-stimulating factor and erythropoietin. Br J Haematol 97:309–311
2. Dokal I (2000) Dyskeratosis congenita in all its forms. Br J Haematol 110:168–179
3. Dokal I, Vulliamy T (2003) Dyskeratosis congenita: its link to telomerase and aplastic anaemia. Blood Rev 17:217–225
4. Knight SW Heiss NS, Vulliamy TJ et al. (1999) X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. Am J Hum Genet 65:50–58
5. Kraemer D, Goebeler M (2003) Missense mutation in a patient with X-linked dyskeratosis congenita. Haematologica 88:ECR 11
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