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...

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Detaylı Bibliyografya
Yayımlandı:Br J Haematol
Asıl Yazarlar: Shen, Wenyi, Kerr, Cassandra M., Przychozen, Bartlomiej, Mahfouz, Reda Z., LaFramboise, Thomas, Nagata, Yasunobu, Hanna, Rabi, Radivoyevitch, Tomas, Nazha, Aziz, Sekeres, Mikkael A., Maciejewski, Jaroslaw P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2019
Konular:
Article
Online Erişim: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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