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Impact of germline CTC1 alterations on telomere length in acquired bone marrow failure
Compound heterozygous germline mutations in CTC1 gene have been found in patients with atypical dyskeratosis congenita (DC), whereas heterozygous carriers are unaffected. Through screening of a large cohort of adult patients with acquired bone marrow failure syndromes, in addition to a DC case, we h...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Br J Haematol |
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| Κύριοι συγγραφείς: | , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6536344/ https://ncbi.nlm.nih.gov/pubmed/30891747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjh.15862 |
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