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TIN2 Protein Dyskeratosis Congenita Missense Mutants Are Defective in Association with Telomerase
Dyskeratosis congenita (DC) is a progressive and heterogeneous congenital disorder that affects multiple systems and is characterized by bone marrow failure and a triad of abnormal skin pigmentation, nail dystrophy, and oral leukoplakia. One common feature for all DC patients is abnormally short tel...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
American Society for Biochemistry and Molecular Biology
2011
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3123070/ https://ncbi.nlm.nih.gov/pubmed/21536674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.225870 |
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