Dyskeratosis congenita: a disorder of telomerase deficiency and its relationship to other diseases
Author:
Publisher
Informa UK Limited
Subject
Dermatology
Link
http://www.tandfonline.com/doi/pdf/10.1586/17469872.1.3.463
Reference122 articles.
1. Dyskeratosis Congenita
2. A disease of premature ageing
3. Dyskeratosis congenita: molecular insights into telomerase function, ageing and cancer
4. Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation
5. X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
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1. Oral and Dental Findings of the Longest Surviving Patient with Hoyeraal-Hreidarsson Syndrome;Journal of Oral Health and Community Dentistry;2014-01
2. Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia;Human Mutation;2009-11
3. Circulating haematopoietic progenitors are differentially reduced amongst subtypes of dyskeratosis congenita;British Journal of Haematology;2008-03
4. Dyskeratosis Congenita: A historical perspective;Mechanisms of Ageing and Development;2008-01
5. Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome;Blood;2007-12-15
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