Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome

Author:

Habib Raneem12,Kim Ryong23,Neitzel Heidemarie2,Demuth Ilja45,Chrzanowska Krystyna6,Seemanova Eva7,Faber Renaldo8,Digweed Martin2,Voss Reinhard9,Jäger Kathrin1011,Sperling Karl2,Walter Michael1011

Affiliation:

1. Department of Human Genetics, Ruhr-University Bochum, Bochum, Germany

2. Institute of Medical and Human Genetics, Charité - Universitätsmedizin Berlin, Berlin, Germany

3. Institute of Clinical Chemistry, Red-Cross General Hospital, Pyongyang, Democratic People’s Republic of Korea

4. Department of Endocrinology and Metabolism, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Germany

5. Charité - Universitätsmedizin Berlin, BCRT - Berlin Institute of Health Center for Regenerative Therapies, Berlin, Germany

6. Department of Medical Genetics, The Children’s Memorial Health Institute, Warsaw, Poland

7. Department of Clinical Genetics, Institute of Biology and Medical Genetics, Second Medical School, Charles University, Prague, Czech Republic

8. Center for Prenatal Medicine, Leipzig, Germany

9. Integrated Functional Genomics, Interdisciplinary Center for Clinical Research, University of Münster, Münster, Germany

10. Institute of Clinical Chemistry and Laboratory Medicine, University of Rostock, Rostock, Germany

11. Institute of Laboratory Medicine, Clinical Chemistry and Pathobiochemistry, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Germany

Publisher

Impact Journals, LLC

Subject

Cell Biology,Aging

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